<?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>S1870-249X2006000400001</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Investigation of NQR Parameters on the Tetrazole-Azide Tautomeric Equilibria: A DFT Study]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Monajjemi]]></surname>
<given-names><![CDATA[Majid]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Honarparvar]]></surname>
<given-names><![CDATA[Bahareh]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Monajemi]]></surname>
<given-names><![CDATA[Hadieh]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Islamic Azad University Science and Research Branch ]]></institution>
<addr-line><![CDATA[Teherán ]]></addr-line>
<country>Irán</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Islamic Azad University Department of Physics ]]></institution>
<addr-line><![CDATA[Teherán ]]></addr-line>
<country>Irán</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2006</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2006</year>
</pub-date>
<volume>50</volume>
<numero>4</numero>
<fpage>143</fpage>
<lpage>148</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2006000400001&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2006000400001&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2006000400001&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[A theoretical study was undertaken to reinvestigate whether NQR parameters such as quadrupole coupling constant, asymmetry factor, and NQR frequencies obtained from electric field gradient tensor can provide information to infer about the substituent effect on tautomeric forms of tetrazole-azide equilibria in a gas phase. For this purpose, 14N-NQR parameters of 5-R -tetrazolo [1, 5-a] pyridines and its corresponding tautomer, on the tetrazole-azide isomerization, were calculated at the B3LYP/6-31++G** level of theory and compared with each other, where R= H, CH3, OH, Cl, OCH3, NO2. The results reveal that NQR parameters of nitrogen atoms of these compounds are highly sensitive to substituent effects. The influence of these groups on the transition state (TS) was also studied. Moreover, according to some plotted graphs reasonable relationship has been found between the values of the Hammett constant (&#963;p) of mentioned substituents and their 14N-NQR parameter data. In general, it is observed that groups which stabilize the azide isomer lower the Eact of the isomerization reaction, and conversely, those that favor the tetrazole form, raise the Eact , relative to the unsubstituted compound. The TS has a close resemblance to the tetrazole structure. Also, the energy differences between tautomeric forms, the graphs of &#963;p versus energy values, and the graph of Hammett-constants versus Eact as well as the graph of rN3-N4 versus Eact have been analyzed. Finally, we have focused on some critical points in the plotted graphs of both E±Q (J) versus v±Q (MHz) and E±Q (J) versus &#951;.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Se llevó a cabo un estudio teórico para reinvestigar si los parámetros de Resonancia Cuadrupolar Nuclear (RCN) tales como la constante de acoplamiento cuadrupolar, el factor de asimetría y las frecuencias RCN, obtenidos a partir del tensor gradiente del campo eléctrico, pueden proveer información para realizar inferencias sobre los efectos del sustituyente en las formas tautoméricas del equilibrio tetrazol-azida en fase gaseosa. Para este propósito, los parámetros 14N RCN del 5-R tetrazolo [1,5-a] piridinas y su tautómero correspondiente, en la isomerización tetrazol-azida, fueron calculados en el nivel de teoría B3LYP/6-31++G**, y fueron comparados uno con otro, donde R = H, CH3, OH, Cl, OCH3, NO2. Los resultados revelan que los parámetros de los átomos de nitrógeno de estos compuestos son altamente sensibles a los efectos del sustituyente. La influencia de estos grupos en el estado de transición (ET) también fue estudiada. Además, de acuerdo a las gráficas, se encontró una relación razonable entre la constante de Hammett (&#963;p) de los sustituyentes y sus datos derivados de los parámetros 14N- Rp CN. En general, se observa que grupos que estabilizan el isómero azida bajan la Eact de la reacción de isomerización, y complementariamente, aquellos que favorecen la forma de tetrazol, aumentan la E de la reacción, relativo al compuesto sin sustitución. El ET tiene similitud a la estructura del tetrazol. Las diferencias de energía entre las formas tautoméricas fueron evaluadas y las gráficas de &#963;p contra los valores de energía, y la gráfica de constantes de Hammett contra Eact, así como la gráfica rN3-N4 versus Eact, fueron analizadas. Finalmente, hemos enfocado algunos puntos críticos en el trazo de los gráficos de E±Q (J) versus v±Q (MHz) y E±Q (J) versus &#951;.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Tetrazole]]></kwd>
<kwd lng="en"><![CDATA[Tautomeric equilibrium]]></kwd>
<kwd lng="en"><![CDATA[14N-NQR parameters]]></kwd>
<kwd lng="en"><![CDATA[DFT]]></kwd>
<kwd lng="en"><![CDATA[Hammett Constant]]></kwd>
<kwd lng="es"><![CDATA[Tetrazol]]></kwd>
<kwd lng="es"><![CDATA[equilibrio tautomérico]]></kwd>
<kwd lng="es"><![CDATA[parámetros 14N RCN]]></kwd>
<kwd lng="es"><![CDATA[TFD]]></kwd>
<kwd lng="es"><![CDATA[constante de Hammett]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  	    <p align="justify"><font face="verdana" size="4">Article</font></p> 	    <p align="justify">&nbsp;</p> 	    <p align="center"><font face="verdana" size="4"><b>Investigation of NQR Parameters on the Tetrazole&#45;Azide Tautomeric Equilibria: A DFT Study</b></font></p> 	    <p align="justify">&nbsp;</p> 	    <p align="center"><font face="verdana" size="2"><b>Majid Monajjemi,<sup>1</sup>* Bahareh Honarparvar,<sup>1</sup> Hadieh Monajemi<sup>2</sup></b></font></p> 	    <p align="justify">&nbsp;</p> 	    <p align="justify"><font face="verdana" size="2"><sup><i>1</i></sup><i>&nbsp;Science and Research Branch, Islamic Azad University, P. O .Box 14515&#45;775, Tehran, Iran. Email:</i> <a href="mailto:m_monajjemi@yahoo.com">m_monajjemi@yahoo.com</a></font></p> 	    <p align="justify"><font face="verdana" size="2"><sup><i>2</i></sup><i>&nbsp;Department of Physics, Karaj Branch, Islamic Azad University, Karaj, Tehran, Iran</i></font></p> 	    <p align="justify">&nbsp;</p> 	    ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">Recibido el 11 de mayo del 2006.     <br>     Aceptado el 28 de septiembre del 2006.</font></p> 	    <p align="justify">&nbsp;</p> 	    <p align="justify"><font face="verdana" size="2"><b>Abstract</b></font></p> 	    <p align="justify"><font face="verdana" size="2"> A theoretical study was undertaken to reinvestigate whether NQR parameters such as quadrupole coupling constant, asymmetry factor, and NQR frequencies obtained from electric field gradient tensor can provide information to infer about the substituent effect on tautomeric forms of tetrazole&#45;azide equilibria in a gas phase. For this purpose, <sup>14</sup>N&#45;NQR parameters of 5&#45;R &#45;tetrazolo &#91;1, 5&#45;a&#93; pyridines and its corresponding tautomer, on the tetrazole&#45;azide isomerization, were calculated at the B3LYP/6&#45;31++G** level of theory and compared with each other, where R= H, CH<sub>3</sub>, OH, Cl, OCH<sub>3</sub>, NO<sub>2</sub>. The results reveal that NQR parameters of nitrogen atoms of these compounds are highly sensitive to substituent effects. The influence of these groups on the transition state (TS) was also studied. Moreover, according to some plotted graphs reasonable relationship has been found between the values of the Hammett constant (&sigma;<sub>p</sub>) of mentioned substituents and their <sup>14</sup>N&#45;NQR parameter data. In general, it is observed that groups which stabilize the azide isomer lower the E<sub>act</sub> of the isomerization reaction, and conversely, those that favor the tetrazole form, raise the E<sub>act</sub> , relative to the unsubstituted compound. The TS has a close resemblance to the tetrazole structure. Also, the energy differences between tautomeric forms, the graphs of  &sigma;<sub>p</sub> versus energy values, and the graph of Hammett&#45;constants versus E<sub>act</sub> as well as the graph of r<sub>N3&#45;N4</sub> versus E<sub>act</sub> have been analyzed. Finally, we have focused on some critical points in the plotted graphs of both E<sup>&plusmn;</sup><sub>Q</sub> (J) versus <i>v<sup>&plusmn;</sup></i><sub>Q</sub> (MHz) and E&plusmn;<sub>Q</sub> (J) versus &eta;.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Keywords:</b> Tetrazole; Tautomeric equilibrium; <sup>14</sup>N&#45;NQR parameters; DFT; Hammett Constant.</font></p> 	    <p align="justify">&nbsp;</p> 	    <p align="justify"><font face="verdana" size="2"><b>Resumen</b></font></p> 	    <p align="justify"><font face="verdana" size="2"> Se llev&oacute; a cabo un estudio te&oacute;rico para reinvestigar si los par&aacute;metros de Resonancia Cuadrupolar Nuclear (RCN) tales como la constante de acoplamiento cuadrupolar, el factor de asimetr&iacute;a y las frecuencias RCN, obtenidos a partir del tensor gradiente del campo el&eacute;ctrico, pueden proveer informaci&oacute;n para realizar inferencias sobre los efectos del sustituyente en las formas tautom&eacute;ricas del equilibrio tetrazol&#45;azida en fase gaseosa. Para este prop&oacute;sito, los par&aacute;metros <sup>14</sup>N RCN del 5&#45;R tetrazolo &#91;1,5&#45;a&#93; piridinas y su taut&oacute;mero correspondiente, en la isomerizaci&oacute;n tetrazol&#45;azida, fueron calculados en el nivel de teor&iacute;a B3LYP/6&#45;31++G**, y fueron comparados uno con otro, donde R = H, CH<sub>3</sub>, OH, Cl, OCH<sub>3</sub>, NO<sub>2</sub>. Los resultados revelan que los par&aacute;metros de los &aacute;tomos de nitr&oacute;geno de estos compuestos son altamente sensibles a los efectos del sustituyente. La influencia de estos grupos en el estado de transici&oacute;n (ET) tambi&eacute;n fue estudiada. Adem&aacute;s, de acuerdo a las gr&aacute;ficas, se encontr&oacute; una relaci&oacute;n razonable entre la constante de Hammett (&sigma;<sub>p</sub>) de los sustituyentes y sus datos derivados de los par&aacute;metros <sup>14</sup>N&#45; R<sup>p</sup> CN. En general, se observa que grupos que estabilizan el is&oacute;mero azida bajan la E<sub>act</sub> de la reacci&oacute;n de isomerizaci&oacute;n, y complementariamente, aquellos que favorecen la forma de tetrazol, aumentan la E de la reacci&oacute;n, relativo al compuesto sin sustituci&oacute;n. El ET tiene similitud a la estructura del tetrazol. Las diferencias de energ&iacute;a entre las formas tautom&eacute;ricas fueron evaluadas y las gr&aacute;ficas de &sigma;<sub>p</sub> contra los valores de energ&iacute;a, y la gr&aacute;fica de constantes de Hammett contra E<sub>act</sub>, as&iacute; como la gr&aacute;fica r<sub>N3&#45;N4</sub> </font><font face="verdana" size="2">versus E<sub>act</sub>, fueron analizadas. Finalmente, hemos enfocado algunos puntos cr&iacute;ticos en el trazo de los gr&aacute;ficos de E&plusmn;<sub>Q</sub> (J) versus v<sup>&plusmn;</sup><sub>Q</sub> (MHz) y E&plusmn;<sub>Q</sub> (J) versus  &eta;.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Palabras clave:</b> Tetrazol, equilibrio tautom&eacute;rico, par&aacute;metros <sup>14</sup>N RCN, TFD, constante de Hammett. </font></p>     ]]></body>
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