<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0035-001X</journal-id>
<journal-title><![CDATA[Revista mexicana de física]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. mex. fis.]]></abbrev-journal-title>
<issn>0035-001X</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Mexicana de Física]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0035-001X2023000500018</article-id>
<article-id pub-id-type="doi">10.31349/revmexfis.69.051701</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Standard molar enthalpies of formation of 3-methylglutaric and 3,3-dimethylglutaric anhydrides]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[García-Castro]]></surname>
<given-names><![CDATA[M. A.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Díaz-Sánchez]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Galicia-Aguilar]]></surname>
<given-names><![CDATA[J. A.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vidal-Robles]]></surname>
<given-names><![CDATA[E.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Benemérita Universidad Autónoma de Puebla Facultad de Ingeniería Química ]]></institution>
<addr-line><![CDATA[Puebla Pue,]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>10</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>10</month>
<year>2023</year>
</pub-date>
<volume>69</volume>
<numero>5</numero>
<fpage>0</fpage>
<lpage>0</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0035-001X2023000500018&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0035-001X2023000500018&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0035-001X2023000500018&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract In this research, both the standard molar enthalpy of formation in the crystalline phase and in the gas phase of 3-methylglutaric anhydride was calculated from experimental data. The temperature and enthalpy of fusion, as well as the molar heat capacity in solid phase was calculated by differential scanning calorimetry; the molar enthalpy of sublimation at 298.15 K by the Knudsen effusion method, the molar enthalpy of vaporization at 298.15 K by thermogravimetric analysis, and the standard massic combustion energy by combustion adiabatic calorimetry. Since 3,3-dimethylglutaric anhydride presented crystal transitions (with endothermic points at 352.76 K, 356.98 K and 397.15 K), some of its thermochemical properties were estimated from the functional group-contribution methods proposed by Benson, Gani and Naef and from application of Machine Learning based models.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[3-methylglutaric anhydride]]></kwd>
<kwd lng="en"><![CDATA[3,3-dimethylglutaric anhydride]]></kwd>
<kwd lng="en"><![CDATA[enthalpy of formation]]></kwd>
<kwd lng="en"><![CDATA[functional group-contribution methods]]></kwd>
</kwd-group>
</article-meta>
</front><back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Maria]]></surname>
<given-names><![CDATA[V. S.]]></given-names>
</name>
<name>
<surname><![CDATA[Line]]></surname>
<given-names><![CDATA[B.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Cyclic anhydrides as powerful tools for bioconjugation and smart delivery]]></article-title>
<source><![CDATA[Bioconjugate Chem.]]></source>
<year>2021</year>
<volume>32</volume>
<page-range>482</page-range></nlm-citation>
</ref>
<ref id="B2">
<label>2</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bardhan]]></surname>
<given-names><![CDATA[J. C.]]></given-names>
</name>
<name>
<surname><![CDATA[Adhya]]></surname>
<given-names><![CDATA[R. N.]]></given-names>
</name>
<name>
<surname><![CDATA[Bhattacharyya]]></surname>
<given-names><![CDATA[K. C.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Synthesis of polycyclic compounds. Part IV. Substituted 3-alkylphenanthrenes]]></article-title>
<source><![CDATA[J. Chem. Soc.]]></source>
<year>1956</year>
<page-range>1346</page-range></nlm-citation>
</ref>
<ref id="B3">
<label>3</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Yamamoto]]></surname>
<given-names><![CDATA[Y.]]></given-names>
</name>
<name>
<surname><![CDATA[Yamamoto]]></surname>
<given-names><![CDATA[K.]]></given-names>
</name>
<name>
<surname><![CDATA[Nishioka]]></surname>
<given-names><![CDATA[T.]]></given-names>
</name>
<name>
<surname><![CDATA[Oda]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Asymmetric synthesis of optically active lactones from cyclic acid anhydrides using lipase in organic solvents]]></article-title>
<source><![CDATA[Agr. Biol. Chem.]]></source>
<year>2014</year>
<volume>52</volume>
<page-range>3087</page-range></nlm-citation>
</ref>
<ref id="B4">
<label>4</label><nlm-citation citation-type="">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Dale]]></surname>
<given-names><![CDATA[R. C.]]></given-names>
</name>
</person-group>
<source><![CDATA[Indoline compounds as granzyme b inhibitors]]></source>
<year>2019</year>
</nlm-citation>
</ref>
<ref id="B5">
<label>5</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Wu]]></surname>
<given-names><![CDATA[T.Y.]]></given-names>
</name>
<name>
<surname><![CDATA[Lai]]></surname>
<given-names><![CDATA[Y. R.]]></given-names>
</name>
<name>
<surname><![CDATA[Tsai]]></surname>
<given-names><![CDATA[S. W.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[CALB-Catalyzed two-step alcoholytic desymmetrization of 3-methylglutaric diazolides in MTBE]]></article-title>
<source><![CDATA[Appl. Biochem. Biotech.]]></source>
<year>2018</year>
<volume>185</volume>
<page-range>578</page-range></nlm-citation>
</ref>
<ref id="B6">
<label>6</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Shim]]></surname>
<given-names><![CDATA[J. H.]]></given-names>
</name>
<name>
<surname><![CDATA[Park]]></surname>
<given-names><![CDATA[S. J.]]></given-names>
</name>
<name>
<surname><![CDATA[Ahn]]></surname>
<given-names><![CDATA[B. K.]]></given-names>
</name>
<name>
<surname><![CDATA[Lee]]></surname>
<given-names><![CDATA[J. Y.]]></given-names>
</name>
<name>
<surname><![CDATA[Kim]]></surname>
<given-names><![CDATA[H. S.]]></given-names>
</name>
<name>
<surname><![CDATA[Ha]]></surname>
<given-names><![CDATA[D. C.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Enantioselective thiolysis and aminolysis of cyclic anhydrides using a chiral diamine-derived thiourea catalyst]]></article-title>
<source><![CDATA[ACS Omega]]></source>
<year>2021</year>
<volume>50</volume>
<page-range>34501</page-range></nlm-citation>
</ref>
<ref id="B7">
<label>7</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Gandhi]]></surname>
<given-names><![CDATA[S. K..]]></given-names>
</name>
<name>
<surname><![CDATA[Schultz]]></surname>
<given-names><![CDATA[J. R.]]></given-names>
</name>
<name>
<surname><![CDATA[Boughey]]></surname>
<given-names><![CDATA[F. W.]]></given-names>
</name>
<name>
<surname><![CDATA[Forsythe]]></surname>
<given-names><![CDATA[R. H.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Chemical modification of egg white with 3,3-dimethylglutaric anhydride]]></article-title>
<source><![CDATA[J. Food Sci.]]></source>
<year>1968</year>
<volume>33</volume>
<page-range>163</page-range></nlm-citation>
</ref>
<ref id="B8">
<label>8</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Yuba]]></surname>
<given-names><![CDATA[E.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Dextran derivative-based pH-sensitive liposomes for cancer immunotherapy]]></article-title>
<source><![CDATA[Biomaterials]]></source>
<year>2014</year>
<volume>35</volume>
<page-range>3091</page-range></nlm-citation>
</ref>
<ref id="B9">
<label>9</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Kobrakov]]></surname>
<given-names><![CDATA[K. L.]]></given-names>
</name>
<name>
<surname><![CDATA[Korolev]]></surname>
<given-names><![CDATA[V. K.]]></given-names>
</name>
<name>
<surname><![CDATA[Rybina]]></surname>
<given-names><![CDATA[L. I.]]></given-names>
</name>
<name>
<surname><![CDATA[Kelarev]]></surname>
<given-names><![CDATA[V. I.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Halogen-containing pyridines. 7. Synthesis and some conversions of (3,5-dichloro-2-pyridyl)hydrazine]]></article-title>
<source><![CDATA[Chem. Heterocycl. Com+]]></source>
<year>2000</year>
<volume>36</volume>
<page-range>931</page-range></nlm-citation>
</ref>
<ref id="B10">
<label>10</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Trang]]></surname>
<given-names><![CDATA[T.]]></given-names>
</name>
<name>
<surname><![CDATA[Nhung]]></surname>
<given-names><![CDATA[N.]]></given-names>
</name>
<name>
<surname><![CDATA[Kobayashi]]></surname>
<given-names><![CDATA[T.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Fabrication and characterization of pulp/chitosan composite membranes crosslinked with 3-methylglutaric anhydride for pervaporation of ethanol/water mixture]]></article-title>
<source><![CDATA[Engineering-London]]></source>
<year>2011</year>
<volume>3</volume>
<page-range>110</page-range></nlm-citation>
</ref>
<ref id="B11">
<label>11</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Salas-López]]></surname>
<given-names><![CDATA[K.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Standard enthalpies of formation of N,N&#8217; -(1,3-phenylene)bis(phthalimide) and N,N&#8217; -(1,3-phenylene)bis(phthalimide-5-carboxilic acid)]]></article-title>
<source><![CDATA[Thermochim. Acta]]></source>
<year>2021</year>
<volume>697</volume>
<page-range>178861</page-range></nlm-citation>
</ref>
<ref id="B12">
<label>12</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Caldera]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
<name>
<surname><![CDATA[García-Castro]]></surname>
<given-names><![CDATA[M. A.]]></given-names>
</name>
<name>
<surname><![CDATA[García]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<name>
<surname><![CDATA[Herrera]]></surname>
<given-names><![CDATA[A. M.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Comparison of polyampholyte derivative of chitosan with bisphtalimides of low molecular weight in the green synthesis of Au nanoparticles]]></article-title>
<source><![CDATA[Gold Bull.]]></source>
<year>2022</year>
<volume>55</volume>
<page-range>41</page-range></nlm-citation>
</ref>
<ref id="B13">
<label>13</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[López-Badillo]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Experimental standard enthalpies of formation 4,4-methylenedi(phenylene isocyanate) and polyamide-imides]]></article-title>
<source><![CDATA[Russ. J. Phys. Chem. B]]></source>
<year>2021</year>
<volume>15</volume>
<page-range>S201</page-range></nlm-citation>
</ref>
<ref id="B14">
<label>14</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[López-Badillo]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Obtaining kinetic parameters of polyamide imide reaction]]></article-title>
<source><![CDATA[Rev. Mex. Ing. Química]]></source>
<year>2019</year>
<volume>19</volume>
<page-range>783</page-range></nlm-citation>
</ref>
<ref id="B15">
<label>15</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Xun]]></surname>
<given-names><![CDATA[Z.]]></given-names>
</name>
<name>
<surname><![CDATA[Chengjian]]></surname>
<given-names><![CDATA[Z.]]></given-names>
</name>
<name>
<surname><![CDATA[Xinghong]]></surname>
<given-names><![CDATA[Z.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[A facile and unprecedented route to a library of thermostable formaldehyde-derived polyesters: highly active and selective copolymerization of cyclic acetals and anhydrides]]></article-title>
<source><![CDATA[Angew. Chem-Ger Edit]]></source>
<year>2022</year>
<volume>61</volume>
</nlm-citation>
</ref>
<ref id="B16">
<label>16</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Jezowski]]></surname>
<given-names><![CDATA[S. R.]]></given-names>
</name>
<name>
<surname><![CDATA[Monaco]]></surname>
<given-names><![CDATA[S.]]></given-names>
</name>
<name>
<surname><![CDATA[Yennawar]]></surname>
<given-names><![CDATA[H. P.]]></given-names>
</name>
<name>
<surname><![CDATA[Wonderling]]></surname>
<given-names><![CDATA[N. M.]]></given-names>
</name>
<name>
<surname><![CDATA[Mathersd]]></surname>
<given-names><![CDATA[R. T.]]></given-names>
</name>
<name>
<surname><![CDATA[Schatschneider]]></surname>
<given-names><![CDATA[B.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Unusual physical behaviour and polymorphic phase transitions in crystalline bicyclic anhydrides]]></article-title>
<source><![CDATA[Cryst. Eng. Comm.]]></source>
<year>2017</year>
<volume>19</volume>
<page-range>276</page-range></nlm-citation>
</ref>
<ref id="B17">
<label>17</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Zhao]]></surname>
<given-names><![CDATA[D.]]></given-names>
</name>
<name>
<surname><![CDATA[Li]]></surname>
<given-names><![CDATA[F. F.]]></given-names>
</name>
<name>
<surname><![CDATA[Zhang]]></surname>
<given-names><![CDATA[A. Y.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Naphthalene-1,8-dicarboxylic anhydride: a monoclinic polymorph]]></article-title>
<source><![CDATA[Acta Cryst.]]></source>
<year>2010</year>
<volume>66</volume>
<page-range>o2622</page-range></nlm-citation>
</ref>
<ref id="B18">
<label>18</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Díaz]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
<name>
<surname><![CDATA[Ramírez V]]></surname>
<given-names><![CDATA[B.]]></given-names>
</name>
<name>
<surname><![CDATA[Velásquez]]></surname>
<given-names><![CDATA[W.]]></given-names>
</name>
<name>
<surname><![CDATA[Rodríguez]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[A new polymorph of 9,10-dihydroanthracene-9,10-&#945;, &#946;-succinic acid anhydride]]></article-title>
<source><![CDATA[Acta Cryst.]]></source>
<year>2002</year>
<volume>58</volume>
<page-range>o501</page-range></nlm-citation>
</ref>
<ref id="B19">
<label>19</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Kuhnert-Brandstatter]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
<name>
<surname><![CDATA[Sollinger]]></surname>
<given-names><![CDATA[H. W.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermal analytical and infrared spectroscopic investigations on polymorphic organic compounds VIII]]></article-title>
<source><![CDATA[Mikrochim. Acta]]></source>
<year>1990</year>
<volume>102</volume>
<page-range>247</page-range></nlm-citation>
</ref>
<ref id="B20">
<label>20</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Pirsch]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Polarity, molar heat of fusion, and melting-point position of organic compounds. Polymorphic transformations in the melting point region and their heats of transformation]]></article-title>
<source><![CDATA[Monat. Chem.]]></source>
<year>1955</year>
<volume>86</volume>
<page-range>216</page-range></nlm-citation>
</ref>
<ref id="B21">
<label>21</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Caira]]></surname>
<given-names><![CDATA[M. R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Crystalline polymorphism of organic compounds]]></article-title>
<source><![CDATA[Topics in Current Chemistry 198]]></source>
<year>1998</year>
<page-range>163</page-range></nlm-citation>
</ref>
<ref id="B22">
<label>22</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Yu]]></surname>
<given-names><![CDATA[L.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[hermochemistry and conformational polymorphism of a hexamorphic crystal system]]></article-title>
<source><![CDATA[J. Am. Chem. Soc.]]></source>
<year>2000</year>
<volume>122</volume>
<page-range>585</page-range></nlm-citation>
</ref>
<ref id="B23">
<label>23</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ahmed]]></surname>
<given-names><![CDATA[E.]]></given-names>
</name>
<name>
<surname><![CDATA[Karothu]]></surname>
<given-names><![CDATA[D. P.]]></given-names>
</name>
<name>
<surname><![CDATA[Pejov]]></surname>
<given-names><![CDATA[L.]]></given-names>
</name>
<name>
<surname><![CDATA[Commins]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
<name>
<surname><![CDATA[Hu]]></surname>
<given-names><![CDATA[Q.]]></given-names>
</name>
<name>
<surname><![CDATA[Naumov]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[From mechanical effects to mechanochemistry: Softening and depression of the melting point of deformed plastic crystal]]></article-title>
<source><![CDATA[J. Am. Chem. Soc.]]></source>
<year>2020</year>
<volume>142</volume>
<page-range>11219</page-range></nlm-citation>
</ref>
<ref id="B24">
<label>24</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Salas-López]]></surname>
<given-names><![CDATA[K.]]></given-names>
</name>
<name>
<surname><![CDATA[Amador]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
<name>
<surname><![CDATA[Rojas]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<name>
<surname><![CDATA[Melende]]></surname>
<given-names><![CDATA[F. J.]]></given-names>
</name>
<name>
<surname><![CDATA[Flores]]></surname>
<given-names><![CDATA[H.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Experimental and theoretical thermochemistry of the isomers 3- and 4-nitrophthalimide]]></article-title>
<source><![CDATA[J. Phys. Chem. A]]></source>
<year>2017</year>
<volume>121</volume>
<page-range>5509</page-range></nlm-citation>
</ref>
<ref id="B25">
<label>25</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Abdul]]></surname>
<given-names><![CDATA[A. G.]]></given-names>
</name>
<name>
<surname><![CDATA[Al-Muslem]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<name>
<surname><![CDATA[Ahmad]]></surname>
<given-names><![CDATA[N.]]></given-names>
</name>
<name>
<surname><![CDATA[Alquaity]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<name>
<surname><![CDATA[Zahid]]></surname>
<given-names><![CDATA[U.]]></given-names>
</name>
<name>
<surname><![CDATA[Ahmed]]></surname>
<given-names><![CDATA[U.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Predicting Enthalpy of Combustion Using Machine Learning]]></article-title>
<source><![CDATA[Processes]]></source>
<year>2022</year>
<volume>10</volume>
<page-range>2384</page-range></nlm-citation>
</ref>
<ref id="B26">
<label>26</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Vatani]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<name>
<surname><![CDATA[Mehrpooya]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
<name>
<surname><![CDATA[Gharagheizi]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Prediction of Standard Enthalpy of Formation by a QSPR Model]]></article-title>
<source><![CDATA[Int. J. Mol. Sci.]]></source>
<year>2007</year>
<volume>8</volume>
<page-range>407</page-range></nlm-citation>
</ref>
<ref id="B27">
<label>27</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Matos]]></surname>
<given-names><![CDATA[M. A. R.]]></given-names>
</name>
<name>
<surname><![CDATA[Miranda]]></surname>
<given-names><![CDATA[M. S.]]></given-names>
</name>
<name>
<surname><![CDATA[Fonseca]]></surname>
<given-names><![CDATA[D. A. P.]]></given-names>
</name>
<name>
<surname><![CDATA[Morais]]></surname>
<given-names><![CDATA[V. M. F.]]></given-names>
</name>
<name>
<surname><![CDATA[Liebman]]></surname>
<given-names><![CDATA[J. F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Calorimetric and Computational Thermochemical Study of 3,3-Tetramethyleneglutaric Acid, 3,3-Tetramethyleneglutaric Anhydride, and 3,3-Tetramethyleneglutarimide]]></article-title>
<source><![CDATA[J. Phys. Chem A]]></source>
<year>2008</year>
<volume>112</volume>
<page-range>10053</page-range></nlm-citation>
</ref>
<ref id="B28">
<label>28</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Sabbah]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Reference materials for calorimetry and differential thermal analysis]]></article-title>
<source><![CDATA[Thermochim. Acta]]></source>
<year>1999</year>
<volume>331</volume>
<page-range>93</page-range></nlm-citation>
</ref>
<ref id="B29">
<label>29</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Plato]]></surname>
<given-names><![CDATA[C.]]></given-names>
</name>
<name>
<surname><![CDATA[Glasgow]]></surname>
<given-names><![CDATA[A. R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Differential scanning calorimetry as a general method for determining the purity and heat of fusion of high-purity organic chemicals. Application to 95 compounds]]></article-title>
<source><![CDATA[J. Anal. Chem.]]></source>
<year>1969</year>
<volume>41</volume>
<page-range>330</page-range></nlm-citation>
</ref>
<ref id="B30">
<label>30</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Brown]]></surname>
<given-names><![CDATA[M. E.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Determination of purity by differential scanning calorimetry (DSC)]]></article-title>
<source><![CDATA[J. Chem. Educ.]]></source>
<year>1979</year>
<volume>56</volume>
<page-range>310</page-range></nlm-citation>
</ref>
<ref id="B31">
<label>31</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Góralski]]></surname>
<given-names><![CDATA[P. a]]></given-names>
</name>
<name>
<surname><![CDATA[Tkaczyk]]></surname>
<given-names><![CDATA[M. a]]></given-names>
</name>
<name>
<surname><![CDATA[Chorazewski]]></surname>
<given-names><![CDATA[M. a]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Heat capacities of &#945;, &#969;-dichloroalkanes at temperatures from 284.15 K to 353.15 K and a group additivity analysis]]></article-title>
<source><![CDATA[J. Chem. Eng. Data.]]></source>
<year>2003</year>
<volume>48</volume>
<page-range>492</page-range></nlm-citation>
</ref>
<ref id="B32">
<label>32</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Coops]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<name>
<surname><![CDATA[Jessup]]></surname>
<given-names><![CDATA[R. S.]]></given-names>
</name>
<name>
<surname><![CDATA[Nes]]></surname>
<given-names><![CDATA[K. G. van]]></given-names>
</name>
<name>
<surname><![CDATA[Rossini]]></surname>
<given-names><![CDATA[F. D.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Experimental Thermochemistry]]></article-title>
<source><![CDATA[N. Y.: Interscience]]></source>
<year>1956</year>
</nlm-citation>
</ref>
<ref id="B33">
<label>33</label><nlm-citation citation-type="">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Wagman]]></surname>
<given-names><![CDATA[D. D.]]></given-names>
</name>
</person-group>
<source><![CDATA[The NBS tables of chemical thermodynamic properties: Selected values for inorganic and C1 and C2 organic substances in SI units, american chemical society and the american institute of physics for the national bureau of standards]]></source>
<year>1982</year>
<publisher-loc><![CDATA[Washington, D.C ]]></publisher-loc>
</nlm-citation>
</ref>
<ref id="B34">
<label>34</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Meija]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Atomic weights of the elements 2013 (IUPAC Technical Report)]]></article-title>
<source><![CDATA[Pure Appl. Chem.]]></source>
<year>2016</year>
<volume>88</volume>
<page-range>265</page-range></nlm-citation>
</ref>
<ref id="B35">
<label>35</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Good]]></surname>
<given-names><![CDATA[W. D.]]></given-names>
</name>
<name>
<surname><![CDATA[Smith]]></surname>
<given-names><![CDATA[N. K.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Enthalpies of combustion of toluene, benzene, cyclohexane, cyclohexene, methylcyclopentane, 1-methylcyclopentene, and n-hexane]]></article-title>
<source><![CDATA[J. Chem. Eng. Data]]></source>
<year>1969</year>
<volume>14</volume>
<page-range>102</page-range></nlm-citation>
</ref>
<ref id="B36">
<label>36</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Price]]></surname>
<given-names><![CDATA[D. M.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Vapor pressure determination by thermogravimetry]]></article-title>
<source><![CDATA[Thermochim. Acta]]></source>
<year>2001</year>
<volume>367</volume>
<page-range>253</page-range></nlm-citation>
</ref>
<ref id="B37">
<label>37</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Vieyra-Eusebio]]></surname>
<given-names><![CDATA[M.T.]]></given-names>
</name>
<name>
<surname><![CDATA[Rojas]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Vapor Pressures and Sublimation Enthalpies of Nickelocene and Cobaltocene Measured by Thermogravimetry]]></article-title>
<source><![CDATA[J. Chem. Eng. Data]]></source>
<year>2011</year>
<volume>56</volume>
<page-range>5008</page-range></nlm-citation>
</ref>
<ref id="B38">
<label>38</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[García-Castro]]></surname>
<given-names><![CDATA[M. A.]]></given-names>
</name>
<name>
<surname><![CDATA[Amador]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
<name>
<surname><![CDATA[Hernández-Pérez]]></surname>
<given-names><![CDATA[J. M.]]></given-names>
</name>
<name>
<surname><![CDATA[Medina-Favela]]></surname>
<given-names><![CDATA[A. E.]]></given-names>
</name>
<name>
<surname><![CDATA[Flores]]></surname>
<given-names><![CDATA[H.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Experimental and computational thermochemistry of 3- and 4-nitrophthalic anhydride]]></article-title>
<source><![CDATA[J. Phys. Chem. A]]></source>
<year>2014</year>
<volume>118</volume>
<page-range>3820</page-range></nlm-citation>
</ref>
<ref id="B39">
<label>39</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ramos]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<name>
<surname><![CDATA[Ledo]]></surname>
<given-names><![CDATA[J. M.]]></given-names>
</name>
<name>
<surname><![CDATA[Flores]]></surname>
<given-names><![CDATA[H.]]></given-names>
</name>
<name>
<surname><![CDATA[Camarillo]]></surname>
<given-names><![CDATA[E. A.]]></given-names>
</name>
<name>
<surname><![CDATA[Carvente]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<name>
<surname><![CDATA[Amador]]></surname>
<given-names><![CDATA[M. P.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Evaluation of sublimation enthalpy by thermogravimetry: Analysis of the diffusion effects in the case of methyl and phenyl substituted hydrantoins]]></article-title>
<source><![CDATA[Thermochim. Acta]]></source>
<year>2017</year>
<volume>655</volume>
<page-range>181</page-range></nlm-citation>
</ref>
<ref id="B40">
<label>40</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Acree]]></surname>
<given-names><![CDATA[W.]]></given-names>
</name>
<name>
<surname><![CDATA[Chickos]]></surname>
<given-names><![CDATA[J. S.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Phase Transition Enthalpy Measurements of Organic and Organometallic Compounds. Sublimation, Vaporization and Fusion Enthalpies From 1880 to 2010]]></article-title>
<source><![CDATA[J. Phys. Chem. Ref. Data]]></source>
<year>2016</year>
<volume>45</volume>
<page-range>033101</page-range></nlm-citation>
</ref>
<ref id="B41">
<label>41</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Rojas]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<name>
<surname><![CDATA[Orozco]]></surname>
<given-names><![CDATA[E.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Measurement of the enthalpies of vaporization and sublimation of solids aromatic hydrocarbons by differential scanning calorimetry]]></article-title>
<source><![CDATA[Thermochim. Acta]]></source>
<year>2003</year>
<volume>405</volume>
<page-range>93</page-range></nlm-citation>
</ref>
<ref id="B42">
<label>42</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Sabbah]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Reference materials for calorimetry and differential thermal analysis]]></article-title>
<source><![CDATA[Thermochim. Acta]]></source>
<year>1999</year>
<volume>331</volume>
<page-range>93</page-range></nlm-citation>
</ref>
<ref id="B43">
<label>43</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Rojas]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<name>
<surname><![CDATA[Vieyra-Eusebio]]></surname>
<given-names><![CDATA[M. T.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Enthalpies of sublimation of ferrocene and nickelocene measured by calorimetry and the method of Langmuir]]></article-title>
<source><![CDATA[J. Chem. Thermodyn]]></source>
<year>2011</year>
<volume>43</volume>
<page-range>1738</page-range></nlm-citation>
</ref>
<ref id="B44">
<label>44</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bradley]]></surname>
<given-names><![CDATA[R. S.]]></given-names>
</name>
<name>
<surname><![CDATA[Cleasby]]></surname>
<given-names><![CDATA[T. G.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[The vapour pressure and lattice energy of some aromatic ring compounds]]></article-title>
<source><![CDATA[J. Chem.Soc.]]></source>
<year>1953</year>
<volume>169</volume>
<page-range>1690</page-range></nlm-citation>
</ref>
<ref id="B45">
<label>45</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Kruif]]></surname>
<given-names><![CDATA[C. G. De]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Enthalpies of sublimation and vapour pressures of 11 polycyclic hydrocarbons]]></article-title>
<source><![CDATA[J. Chem. Thermodyn.]]></source>
<year>1980</year>
<volume>12</volume>
<page-range>243</page-range></nlm-citation>
</ref>
<ref id="B46">
<label>46</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Malaspina]]></surname>
<given-names><![CDATA[L.]]></given-names>
</name>
<name>
<surname><![CDATA[Gigli]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
<name>
<surname><![CDATA[Bardi]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Microcalorimetric determination of the enthalpy of sublimation of benzoic acid and anthracene]]></article-title>
<source><![CDATA[J. Chem. Phys.]]></source>
<year>1973</year>
<volume>59</volume>
<page-range>387</page-range></nlm-citation>
</ref>
<ref id="B47">
<label>47</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Hansen]]></surname>
<given-names><![CDATA[P. C.]]></given-names>
</name>
<name>
<surname><![CDATA[Eckert]]></surname>
<given-names><![CDATA[C. A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[An improved transpiration method for the measurement of very low vapor pressures]]></article-title>
<source><![CDATA[J. Chem. Eng. Data]]></source>
<year>1986</year>
<volume>31</volume>
<page-range>1</page-range></nlm-citation>
</ref>
<ref id="B48">
<label>48</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Klochkov]]></surname>
<given-names><![CDATA[V. P.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[The vapor pressure of some aromatic compounds]]></article-title>
<source><![CDATA[Zh. Fiz. Khim]]></source>
<year>1985</year>
<volume>32</volume>
<page-range>1177</page-range></nlm-citation>
</ref>
<ref id="B49">
<label>49</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Zherikova]]></surname>
<given-names><![CDATA[K. V.]]></given-names>
</name>
<name>
<surname><![CDATA[Verevkin]]></surname>
<given-names><![CDATA[S. P.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Ferrocene: Temperatura adjustments of sublimation and vaporization enthalpies]]></article-title>
<source><![CDATA[Fluid Phase Equilib.]]></source>
<year>2018</year>
<volume>472</volume>
<page-range>196</page-range></nlm-citation>
</ref>
<ref id="B50">
<label>50</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Hukkerikar]]></surname>
<given-names><![CDATA[A.S.]]></given-names>
</name>
<name>
<surname><![CDATA[Meier]]></surname>
<given-names><![CDATA[R.J.]]></given-names>
</name>
<name>
<surname><![CDATA[Sin]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
<name>
<surname><![CDATA[Gani]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[A method to estimate the enthalpy of formation of organic compounds with chemical accuracy]]></article-title>
<source><![CDATA[Fluid Phase Equilib.]]></source>
<year>2013</year>
<volume>348</volume>
<page-range>23</page-range></nlm-citation>
</ref>
<ref id="B51">
<label>51</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Cohen]]></surname>
<given-names><![CDATA[N.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Revised group additivity values for enthalpies of formation (at 298 K) of carbon-hydrogen and carbon-hydrogen-oxygen compounds]]></article-title>
<source><![CDATA[J. Phys. Chem. Ref. Data]]></source>
<year>1996</year>
<volume>25</volume>
<page-range>1411</page-range></nlm-citation>
</ref>
<ref id="B52">
<label>52</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Holmes]]></surname>
<given-names><![CDATA[J. L.]]></given-names>
</name>
<name>
<surname><![CDATA[Aubry]]></surname>
<given-names><![CDATA[C.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Group additivity values for estimating the enthalpy of formation of organic compounds: An update and reappraisal. 1. C, H and O]]></article-title>
<source><![CDATA[J. Phys. Chem A]]></source>
<year>2011</year>
<volume>115</volume>
<page-range>10576</page-range></nlm-citation>
</ref>
<ref id="B53">
<label>53</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Domalski]]></surname>
<given-names><![CDATA[E.S.]]></given-names>
</name>
<name>
<surname><![CDATA[Hearing]]></surname>
<given-names><![CDATA[E.D.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Estimation of the Thermodynamic Properties of C-HN-O-S-Halogen Compounds at 298.15 K]]></article-title>
<source><![CDATA[J. Phys. Chem. Ref. Data]]></source>
<year>1993</year>
<volume>22</volume>
<page-range>805</page-range></nlm-citation>
</ref>
<ref id="B54">
<label>54</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Naef]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[A generally applicable computer algorithm based on the group additivity method for the calculation of seven molecular descriptors: heat of combustion, LogPo/w, LogS, refractivity, polarizability, toxicity and logbb of organic compounds; scope and limits of applicability]]></article-title>
<source><![CDATA[Molecules]]></source>
<year>2015</year>
<volume>20</volume>
<page-range>18279</page-range></nlm-citation>
</ref>
<ref id="B55">
<label>55</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Naef]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
<name>
<surname><![CDATA[Acree Jr]]></surname>
<given-names><![CDATA[W.E.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Calculation of five thermodynamic molecular descriptors by means of a general computer algorithm based on the group-additivity method: standard enthalpies of vaporization, sublimation and solvation, and entropy of fusion of ordinary organic molecules and total phase-change entropy of liquid crystals]]></article-title>
<source><![CDATA[Molecules]]></source>
<year>2017</year>
<volume>22</volume>
<page-range>1059</page-range></nlm-citation>
</ref>
<ref id="B56">
<label>56</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Naqa]]></surname>
<given-names><![CDATA[I. El]]></given-names>
</name>
<name>
<surname><![CDATA[Murphy]]></surname>
<given-names><![CDATA[M.J.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[What is machine learning?]]></article-title>
<source><![CDATA[Machine Learning in Radiation Oncology: Theory and Applications]]></source>
<year>2015</year>
<volume>17</volume>
<page-range>3</page-range></nlm-citation>
</ref>
<ref id="B57">
<label>57</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Su]]></surname>
<given-names><![CDATA[X.]]></given-names>
</name>
<name>
<surname><![CDATA[Yan]]></surname>
<given-names><![CDATA[X.]]></given-names>
</name>
<name>
<surname><![CDATA[Tsai]]></surname>
<given-names><![CDATA[C.L.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Linear Regression]]></article-title>
<source><![CDATA[WIREs Comput Stat]]></source>
<year>2012</year>
<volume>4</volume>
<page-range>275</page-range></nlm-citation>
</ref>
<ref id="B58">
<label>58</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[McDonald]]></surname>
<given-names><![CDATA[G.C.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Ridge Regression]]></article-title>
<source><![CDATA[Inc. WIREs Comp Stat]]></source>
<year>2009</year>
<volume>1</volume>
<page-range>93</page-range></nlm-citation>
</ref>
<ref id="B59">
<label>59</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ranstam]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<name>
<surname><![CDATA[Cook]]></surname>
<given-names><![CDATA[J.A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[LASSO Regression]]></article-title>
<source><![CDATA[British Journal of Surgery]]></source>
<year>2018</year>
<volume>105</volume>
<page-range>1348</page-range></nlm-citation>
</ref>
<ref id="B60">
<label>60</label><nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Cox]]></surname>
<given-names><![CDATA[J. D.]]></given-names>
</name>
<name>
<surname><![CDATA[Wagman]]></surname>
<given-names><![CDATA[D. D.]]></given-names>
</name>
<name>
<surname><![CDATA[Medvedev]]></surname>
<given-names><![CDATA[V. A.]]></given-names>
</name>
</person-group>
<source><![CDATA[CODATA key values for thermodynamics]]></source>
<year>1989</year>
<publisher-name><![CDATA[Hemisphere Pub. Corp.]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B61">
<label>61</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Roux]]></surname>
<given-names><![CDATA[M. V.]]></given-names>
</name>
<name>
<surname><![CDATA[Temprado]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
<name>
<surname><![CDATA[Chickos]]></surname>
<given-names><![CDATA[J. S.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Vaporization, fusion and sublimation enthalpies of the dicarboxylic acids from C4 to C14 and C16]]></article-title>
<source><![CDATA[J. Chem. Thermodynamics]]></source>
<year>2005</year>
<volume>37</volume>
<page-range>941</page-range></nlm-citation>
</ref>
<ref id="B62">
<label>62</label><nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[CAS]]></surname>
<given-names><![CDATA[Scifinder]]></given-names>
</name>
</person-group>
<source><![CDATA[Substance identifier (value calculated using Advanced Chemistry Development (ACD/Labs), Software V11.02]]></source>
<year>2022</year>
<publisher-name><![CDATA[ACD/Labs]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B63">
<label>63</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Sousa]]></surname>
<given-names><![CDATA[C.]]></given-names>
</name>
<name>
<surname><![CDATA[Matos]]></surname>
<given-names><![CDATA[M. A. R.]]></given-names>
</name>
<name>
<surname><![CDATA[Morais]]></surname>
<given-names><![CDATA[V. M. F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Experimental and Computational Thermochemical Study of Maleic Anhydride and Vinylene Carbonate]]></article-title>
<source><![CDATA[J. Phys. Chem A]]></source>
<year>2017</year>
<volume>121</volume>
<page-range>9474</page-range></nlm-citation>
</ref>
<ref id="B64">
<label>64</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Meng-Yan]]></surname>
<given-names><![CDATA[Y.]]></given-names>
</name>
<name>
<surname><![CDATA[Plicher]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Enthalpies of combustion of succinic anhydride, glutaric anhydride and glutarimide]]></article-title>
<source><![CDATA[J.Chem. Thermodynamics]]></source>
<year>1990</year>
<volume>22</volume>
<page-range>893</page-range></nlm-citation>
</ref>
<ref id="B65">
<label>65</label><nlm-citation citation-type="">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Pedley]]></surname>
<given-names><![CDATA[J. B.]]></given-names>
</name>
<name>
<surname><![CDATA[Naylor]]></surname>
<given-names><![CDATA[R. D.]]></given-names>
</name>
<name>
<surname><![CDATA[Kirby]]></surname>
<given-names><![CDATA[S. P.]]></given-names>
</name>
</person-group>
<source><![CDATA[Thermochemical Data of Organic Compounds, computer analysed thermochemical data]]></source>
<year>1986</year>
<volume>IV</volume>
</nlm-citation>
</ref>
<ref id="B66">
<label>66</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Cox]]></surname>
<given-names><![CDATA[J. D.]]></given-names>
</name>
<name>
<surname><![CDATA[Plicher]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermochemistry or organic and organometallic compounds]]></article-title>
<source><![CDATA[NIST Chemistry Web Book]]></source>
<year>1970</year>
<volume>69</volume>
<page-range>1</page-range></nlm-citation>
</ref>
<ref id="B67">
<label>67</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Steele]]></surname>
<given-names><![CDATA[W. V.]]></given-names>
</name>
<name>
<surname><![CDATA[Charico]]></surname>
<given-names><![CDATA[R. D.]]></given-names>
</name>
<name>
<surname><![CDATA[Cowell]]></surname>
<given-names><![CDATA[A. B.]]></given-names>
</name>
<name>
<surname><![CDATA[Knipmeyer]]></surname>
<given-names><![CDATA[S. E.]]></given-names>
</name>
<name>
<surname><![CDATA[Nguyen]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermodynamic Properties and Ideal-Gas Enthalpies of Formation for 1,4-Diisopropylbenzene, 1,2,4,5-Tetraisopropylbenzene, Cyclohexanone Oxime, Dimethyl Malonate, Glutaric Acid, and Pimelic Acid]]></article-title>
<source><![CDATA[J. Chem. Eng. Data]]></source>
<year>2002</year>
<volume>47</volume>
<page-range>725</page-range></nlm-citation>
</ref>
<ref id="B68">
<label>68</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Vatani]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<name>
<surname><![CDATA[Mehrpooya]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
<name>
<surname><![CDATA[Gharagheizi]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Prediction of Standard Enthalpy of Formation by a QSPR Model]]></article-title>
<source><![CDATA[Int. J. Mol. Sci]]></source>
<year>2007</year>
<volume>8</volume>
<page-range>407</page-range></nlm-citation>
</ref>
<ref id="B69">
<label>69</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Douglas]]></surname>
<given-names><![CDATA[B.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Computational Methods in Organic Thermochemistry. 2. Enthalpies and Free Energies of Formation for Functional Derivatives of Organic Hydrocarbons]]></article-title>
<source><![CDATA[J. Org. Chem.]]></source>
<year>2007</year>
<volume>72</volume>
<page-range>7313</page-range></nlm-citation>
</ref>
<ref id="B70">
<label>70</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ribeiro da Silva]]></surname>
<given-names><![CDATA[M. A. V.]]></given-names>
</name>
<name>
<surname><![CDATA[Cabral]]></surname>
<given-names><![CDATA[J. I. T. A.]]></given-names>
</name>
<name>
<surname><![CDATA[Gomes]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
<name>
<surname><![CDATA[Gomes]]></surname>
<given-names><![CDATA[J. R. B.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Combined Experimental and Computational Study of the Thermochemistry of Methylpiperidines]]></article-title>
<source><![CDATA[J. Org. Chem.]]></source>
<year>2006</year>
<volume>71</volume>
<page-range>3677</page-range></nlm-citation>
</ref>
<ref id="B71">
<label>71</label><nlm-citation citation-type="">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Good]]></surname>
<given-names><![CDATA[W.]]></given-names>
</name>
</person-group>
<source><![CDATA[J. Chem. Eng. Data]]></source>
<year>1972</year>
<volume>17</volume>
<page-range>28</page-range></nlm-citation>
</ref>
<ref id="B72">
<label>72</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Verevkin]]></surname>
<given-names><![CDATA[S. P.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Thermochemistry of amines: experimental standard molar enthalpies of formation of some aliphatic and aromatic amines]]></article-title>
<source><![CDATA[J. Chem. Thermodyn]]></source>
<year>1997</year>
<volume>29</volume>
<page-range>891</page-range></nlm-citation>
</ref>
<ref id="B73">
<label>73</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Geladi]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
<name>
<surname><![CDATA[Kowalski]]></surname>
<given-names><![CDATA[B.R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Partial least squares regression: a tutorial]]></article-title>
<source><![CDATA[Anal Chim Acta]]></source>
<year>1986</year>
<volume>187</volume>
<page-range>1</page-range></nlm-citation>
</ref>
<ref id="B74">
<label>74</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Pendashteh]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Modeling of membrane bioreactor treating hypersaline oily wastewater by artificial neural network]]></article-title>
<source><![CDATA[J. Hazard Mater]]></source>
<year>2011</year>
<volume>192</volume>
<page-range>568</page-range></nlm-citation>
</ref>
<ref id="B75">
<label>75</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Chai]]></surname>
<given-names><![CDATA[T.]]></given-names>
</name>
<name>
<surname><![CDATA[Draxler]]></surname>
<given-names><![CDATA[R.R.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Root mean square error (RMSE) or mean absolute error (MAE)?]]></article-title>
<source><![CDATA[Geosci. Model Dev. Discuss.]]></source>
<year>2014</year>
<volume>7</volume>
<page-range>1525</page-range></nlm-citation>
</ref>
<ref id="B76">
<label>76</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Jung]]></surname>
<given-names><![CDATA[Y.]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Multiple predicting K-fold cross-validation for model selection]]></article-title>
<source><![CDATA[J. of Nonparametric Statistics]]></source>
<year>2018</year>
<volume>30</volume>
<page-range>197</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
