<?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>1870-249X</journal-id>
<journal-title><![CDATA[Journal of the Mexican Chemical Society]]></journal-title>
<abbrev-journal-title><![CDATA[J. Mex. Chem. Soc]]></abbrev-journal-title>
<issn>1870-249X</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Química de México A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1870-249X2017000300205</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Study of CH/&#960; Interactions in the Molecular Recognition between Acetyl Galactopyranoside and 6-substituted 2-Methoxypyridines and 2(1H)-Pyridones]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cuetara-Guadarrama]]></surname>
<given-names><![CDATA[Fabián]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ramírez-Gualito]]></surname>
<given-names><![CDATA[Karla]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cuevas]]></surname>
<given-names><![CDATA[Gabriel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Nacional Autónoma de México Instituto de Química Departamento de Fisicoquímica]]></institution>
<addr-line><![CDATA[Mexico City ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Instituto Politécnico Nacional Centro de Nanociencias y Micro y Nanotecnologías ]]></institution>
<addr-line><![CDATA[Mexico City ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2017</year>
</pub-date>
<volume>61</volume>
<numero>3</numero>
<fpage>205</fpage>
<lpage>216</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2017000300205&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2017000300205&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2017000300205&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract. A series of 6-substituted 2-methoxypyridine and 2(1H)-pyridones was designed and synthesized for its evaluation in the molecular recognition of acetyl 2,3,4,6-tetra-O-methyl-&#946;-D-galactopyranoside substrate. 1H-NMR titration (affinity constant K  a determination) and chemical shift perturbation experiments were performed to evaluate the capacity of these receptors to form CH/&#960; interactions with the substrate. The addition of 2-methoxypyridines to the substrate effected up-field shift for the H3, H4 and H5 proton signals and down-field shift for the H2 proton signal of galactopyranoside substrate. The determined affinity constant K  a values for the association between 2(1H)-pyridones and galactopyranoside showed that molecular recognition was weak. These results have demonstrated the existence of weak CH/&#960; interactions and have reflected their weak intermolecular nature. Finally DFT calculations were performed to illustrate the geometry of the molecular recognition between 2(1H)-pyridones and galactopyranoside.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen. Se diseñó y sintetizó una serie de receptores 2(1H)-piridonas 6-sustiuídos así como sus derivados 2-metoxipiridnas para su evaluación en el reconocimiento molecular del sustrato acetil 2,3,4,6-tetra-O-metil-&#946;-D-galactopiranósido. Se realizaron experimentos en 1H-RMN de titulación (determinación de la constante de afinidad K  a ) y de perturbación del desplazamiento químico con el fin de evaluar la capacidad que tienen estos receptores para formar interacciones CH/&#960; con el sustrato. La adición de 2-metoxipridinas al sustrato provocó el desplazamiento a campos altos de las señales de los protones H3, H4 y H5 y el desplazamiento a campos bajos de la señal del protón H2 del sustrato. Los valores de afinidad K  a determinados para la asociación entre las 2(1H)-piridonas y el galactopiranósido mostraron que el reconocimiento molecular resultó muy débil, como es de esperarse. Estos resultados demostraron la existencia de las interacciones CH/&#960; y reflejaron su naturaleza de fuerzas intermoleculares débiles. Finalmente se hicieron cálculos DFT para demostrar la geometría del reconocimiento molecular entre las 2(1H)-piridonas y el galactopiranósido.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[CH/&#960; interactions]]></kwd>
<kwd lng="en"><![CDATA[supramolecular chemistry]]></kwd>
<kwd lng="en"><![CDATA[glycosides]]></kwd>
<kwd lng="en"><![CDATA[non-covalent interactions]]></kwd>
<kwd lng="en"><![CDATA[molecular recognition]]></kwd>
<kwd lng="es"><![CDATA[interacciones CH/&#960;]]></kwd>
<kwd lng="es"><![CDATA[química supramolecular]]></kwd>
<kwd lng="es"><![CDATA[glicósidos]]></kwd>
<kwd lng="es"><![CDATA[interacciones no-covalentes]]></kwd>
<kwd lng="es"><![CDATA[reconocimiento molecular]]></kwd>
</kwd-group>
</article-meta>
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