<?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>S1870-249X2017000400336</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Luminescence Based Detection of Trinitrophenol and Aromatic Organophosphorous Pesticides Using a Coordination Polymer]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Kaur]]></surname>
<given-names><![CDATA[Rupinder]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Chhibber]]></surname>
<given-names><![CDATA[Manmohan]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mahata]]></surname>
<given-names><![CDATA[Partha]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mittal]]></surname>
<given-names><![CDATA[Susheel K.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Thapar University School of Chemistry & Biochemistry ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>India</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Jadavpur University Department of Chemistry ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>India</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2017</year>
</pub-date>
<volume>61</volume>
<numero>4</numero>
<fpage>336</fpage>
<lpage>341</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2017000400336&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2017000400336&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2017000400336&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Resumen: Las propiedades fluorescentes del polímero de coordinación (CP), 1, fueron utilizadas como detectores de encendido y apagado, para pesticidas nitroaromáticos y organofosforados, respectivamente. El compuesto 1 muestra una eficiencia extraordinariamente alta para la detección del 2,4,6-trinitrofenol (TNP) utilizando la atenuación de la luminiscencia , con un valor de la constante de atenuación [KSV] de 2.30 X 105 M-1, la más alta entre los polímeros de coordinación conocidos. El límite de detección obtenido para el método propuesto fue de 43 ppb. La propiedad de emisión del compuesto 1 fue también utilizada exitósamente para detectar el triazofos y cloropirifos, pesticidas órganofosforados aromáticos, los cuales incrementan la intensidad de emisión en un 238% y un desplazamiento hacia el rojo de ~70 nm, para el primer compuesto. Los pesticidas no aromáticos como el malatión y el acefato no mostraron un incremento en la intensidad de emisión. Los límites de detección para triazofos y cloropirifos, pesticidas órgano osforados aromáticos, fueron de 0.6 and 0.7 ppm, respectivamente.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract: The fluorescent properties of a coordination polymer (CP), 1, were used as turn-on and turn-off detector for nitroaromatics and organophosporus pesticides respectively. Compound 1 exhibits exceptionally high efficiency for the detection of 2,4,6-trinitrophenol (TNP) through luminescence quenching with a quenching constant [KSV] value of 2.30 X 105 M-1, highest among the known coordination polymers. Minimum detection limit achieved by the proposed method was 43 ppb. This emission property of 1 was also used successfully to detect triazophos and chlorpyrifos, aromatic organophosphorus pesticides, which enhanced the emission intensity by 238% and a red shift of ~70 nm in case of former. Non aromatic pesticides like malathion and acephate did not show any increase in the emission intensity. Minimum detection limits for triazophos and chlorpyrifos, aromatic organophosphorus pesticides, were 0.6 and 0.7 ppm respectively.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[nitro-explosives]]></kwd>
<kwd lng="en"><![CDATA[TNT]]></kwd>
<kwd lng="en"><![CDATA[acetylcholinesterases]]></kwd>
<kwd lng="en"><![CDATA[acetylcholine]]></kwd>
<kwd lng="en"><![CDATA[molecular sensing]]></kwd>
<kwd lng="en"><![CDATA[MOF]]></kwd>
<kwd lng="es"><![CDATA[nitro-explosivos]]></kwd>
<kwd lng="es"><![CDATA[TNT]]></kwd>
<kwd lng="es"><![CDATA[acetilcolinesterasas]]></kwd>
<kwd lng="es"><![CDATA[acetilcolina]]></kwd>
<kwd lng="es"><![CDATA[detección molecular]]></kwd>
<kwd lng="es"><![CDATA[MOF]]></kwd>
</kwd-group>
</article-meta>
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