<?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>S1870-249X2009000400002</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Crown Ether Ditopic Receptors for Ammonium Salts with High Affinity for Amino Acid Ester Salts]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rosete-Luna]]></surname>
<given-names><![CDATA[Sharon]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Medrano]]></surname>
<given-names><![CDATA[Felipe]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bernal-Uruchurtu]]></surname>
<given-names><![CDATA[Margarita I.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Godoy-Alcántar]]></surname>
<given-names><![CDATA[Carolina]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad Autónoma del Estado de Morelos Centro de Investigaciones Químicas ]]></institution>
<addr-line><![CDATA[Cuernavaca Morelos]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2009</year>
</pub-date>
<volume>53</volume>
<numero>4</numero>
<fpage>209</fpage>
<lpage>219</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2009000400002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2009000400002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2009000400002&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Two bis crown ether receptors were synthesized and tested as host molecules for protonated forms of alkyl amines and amino acid esters. Molecular recognition studies were conducted in CH2Cl2:MeOH (92:8) by spectrophotometric UV/Vis titrations and by spectrometric ¹H NMR titrations in CDCl3. The calculated binding constants are in the range 10²-10(5) M-1. A high affinity for L-amino acid methyl ester derivatives was found. A theoretical study at the DFT level of the synthesized receptor and some analog ligands with three different ammonium ions helps to rationalize the experimentally found trends.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[En este trabajo se sinterizaron dos receptores del tipo bis eter corona y fueron estudiados como moléculas anfitrión de alquilaminas y ésteres de aminoácidos protonados. Se realizaron estudios de reconocimiento molecular por titulaciones espectrofotométricas UV/Vis en CH2Cl2:MeOH (92:8) y por titulaciones espectrométricas de RMN ¹H en CDCl3. Las constantes de enlace calculadas están en el intervalo 10²-10(5) M-1. Se encontró una alta afinidad por los ésteres metílicos de los L-aminoácidos estudiados. Un estudio teórico a nivel DFT de los receptores sinterizados y algunos ligandos análogos con tres diferentes iones amonio permite explicar las tendencias experimentales encontradas.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Ditopic Receptors]]></kwd>
<kwd lng="en"><![CDATA[Binding Constant]]></kwd>
<kwd lng="en"><![CDATA[Crown Ethers]]></kwd>
<kwd lng="en"><![CDATA[Alkyl Ammonium]]></kwd>
<kwd lng="en"><![CDATA[Amino Acid]]></kwd>
<kwd lng="es"><![CDATA[Receptores ditópicos]]></kwd>
<kwd lng="es"><![CDATA[constante de enlace]]></kwd>
<kwd lng="es"><![CDATA[éteres corona]]></kwd>
<kwd lng="es"><![CDATA[alquilamonio]]></kwd>
<kwd lng="es"><![CDATA[aminoácido]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="justify"><font face="verdana" size="4">Article</font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="4"><b>Crown Ether Ditopic Receptors for Ammonium Salts with High Affinity for Amino Acid Ester Salts</b></font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="2"><b>Sharon Rosete&#150;Luna, Felipe Medrano, Margarita I. Bernal&#150;Uruchurtu, and Carolina Godoy&#150;Alc&aacute;ntar<sup>*</sup></b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><i>Centro de Investigaciones Qu&iacute;micas, Universidad Aut&oacute;noma del Estado de Morelos, 62209 Cuernavaca, Morelos, M&eacute;xico. Tel/Fax: +52 777329 7997. <sup>*</sup>Responsible author:</i> <a href="mailto:cga@uaem.mx">cga@uaem.mx</a></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2">Received August 13, 2009    <br>   Accepted November 19, 2009</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Abstract</b></font></p>     <p align="justify"><font face="verdana" size="2">Two bis crown ether receptors were synthesized and tested as host molecules for protonated forms of alkyl amines and amino acid esters. Molecular recognition studies were conducted in CH<sub>2</sub>Cl<sub>2</sub>:MeOH (92:8) by spectrophotometric UV/Vis titrations and by spectrometric <sup>1</sup>H NMR titrations in CDCl<sub>3</sub>. The calculated binding constants are in the range 10<sup>2</sup>&#150;10<sup>5</sup> M<sup>&#150;1</sup>. A high affinity for L&#150;amino acid methyl ester derivatives was found. A theoretical study at the DFT level of the synthesized receptor and some analog ligands with three different ammonium ions helps to rationalize the experimentally found trends.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Key words: </b>Ditopic Receptors, Binding Constant; Crown Ethers, Alkyl Ammonium, Amino Acid.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Resumen</b></font></p>     <p align="justify"><font face="verdana" size="2">En este trabajo se sinterizaron dos receptores del tipo bis eter corona y fueron estudiados como mol&eacute;culas anfitri&oacute;n de alquilaminas y &eacute;steres de amino&aacute;cidos protonados. Se realizaron estudios de reconocimiento molecular por titulaciones espectrofotom&eacute;tricas UV/Vis en CH<sub>2</sub>Cl<sub>2</sub>:MeOH (92:8) y por titulaciones espectrom&eacute;tricas de RMN <sup>1</sup>H en CDCl<sub>3</sub>. Las constantes de enlace calculadas est&aacute;n en el intervalo 10<sup>2</sup>&#150;10<sup>5</sup> M<sup>&#150;1</sup>. Se encontr&oacute; una alta afinidad por los &eacute;steres met&iacute;licos de los L&#150;amino&aacute;cidos estudiados. Un estudio te&oacute;rico a nivel DFT de los receptores sinterizados y algunos ligandos an&aacute;logos con tres diferentes iones amonio permite explicar las tendencias experimentales encontradas.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Palabras clave: </b>Receptores dit&oacute;picos, constante de enlace, &eacute;teres corona, alquilamonio, amino&aacute;cido.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><a href="/pdf/jmcs/v53n4/v53n4a2.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a> </font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Acknowledgements</b></font></p>     <p align="justify"><font face="verdana" size="2">We thank Professor A. K. Yatsimirsky for the advice and fruitful discussion of the results. SRL thanks CONACyT for the Ph. D. Fellowship. This work was supported by CONACyT, projects 39574-Q and 60747.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>References</b></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">1. Guy, P. A.; Gremaud, E.; Richoz, J.; Turesky, R. J. <i>J. Chromatogr., A </i><b>2000, </b><i>883, </i>89&#150;102.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4912319&pid=S1870-249X200900040000200001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">2. (a) Ohgaki, H.; Takayama, S.; Sugimura, T. <i>Mutat. Res. </i><b>1991, </b><i>259, </i>399&#150;410.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4912321&pid=S1870-249X200900040000200002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --> (b) Wakabayashi, K.; Nagao, M.; Esumi, H.; Sugimura, T. <i>Cancer </i>Res<b>.1992, </b>52, 2092S&#150;2098S.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4912322&pid=S1870-249X200900040000200003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     ]]></body>
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