<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pedras, B.</style></author><author><style face="normal" font="default" size="100%">Oliveira, E.</style></author><author><style face="normal" font="default" size="100%">Santos, H.</style></author><author><style face="normal" font="default" size="100%">Rodriguez, L.</style></author><author><style face="normal" font="default" size="100%">Crehuet, R.</style></author><author><style face="normal" font="default" size="100%">Aviles, T.</style></author><author><style face="normal" font="default" size="100%">Capelo, J. L.</style></author><author><style face="normal" font="default" size="100%">Lodeiro, C.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A new tripodal poly-imine indole-containing ligand: Synthesis, complexation, spectroscopic and theoretical studies</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganica Chimica Acta</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Inorg Chim Acta</style></alt-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">atomic-absorption-spectrometry</style></keyword><keyword><style  face="normal" font="default" size="100%">azomethine ligands</style></keyword><keyword><style  face="normal" font="default" size="100%">derivatives</style></keyword><keyword><style  face="normal" font="default" size="100%">fluorescent chemosensors</style></keyword><keyword><style  face="normal" font="default" size="100%">indole</style></keyword><keyword><style  face="normal" font="default" size="100%">intramolecular excimer formation</style></keyword><keyword><style  face="normal" font="default" size="100%">luminescent sensors</style></keyword><keyword><style  face="normal" font="default" size="100%">macrocyclic ligands</style></keyword><keyword><style  face="normal" font="default" size="100%">metal-ions</style></keyword><keyword><style  face="normal" font="default" size="100%">molecular recognition</style></keyword><keyword><style  face="normal" font="default" size="100%">photophysical properties</style></keyword><keyword><style  face="normal" font="default" size="100%">receptors</style></keyword><keyword><style  face="normal" font="default" size="100%">tripodal ligands</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jun</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://000265509200017</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">8</style></number><volume><style face="normal" font="default" size="100%">362</style></volume><pages><style face="normal" font="default" size="100%">2627-2635</style></pages><isbn><style face="normal" font="default" size="100%">0020-1693</style></isbn><language><style face="normal" font="default" size="100%">English</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;A novel flexible tripodal ligand derived from 3-methylindole, (&quot;InTREN&quot; L), and its mononuclear Zn(II), Cu(II), Ni(II), Hg(II) and Pd(II) complexes are described. All compounds gave analytically pure solid samples. Characterisation of the compounds was accomplished by (1)H NMR, IR and absorption spectroscopies, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) and elemental analysis and their geometry optimized using density functional theory (DFT).Time-dependent-density functional theory (TD-DFT) calculations have been used to assign the lowest energy absorption bands of the free ligand and the Zn(II) complex. The system is a very good candidate for in situ recognition/coordination effects by MALDI-TOF-MS spectrometry and absorption spectroscopy. The presence of three indole groups in InTREN opens up the possibility to synthesize new three-dimensional self-assembly supramolecular structures. (C) 2008 Elsevier B.V. All rights reserved.&lt;/p&gt;
</style></abstract><accession-num><style face="normal" font="default" size="100%">ISI:000265509200017</style></accession-num><notes><style face="normal" font="default" size="100%">&lt;p&gt;437TGTimes Cited:6Cited References Count:52&lt;/p&gt;
</style></notes><auth-address><style face="normal" font="default" size="100%">Rodriguez, LUniv Nova Lisboa, Fac Ciencias &amp; Tecnol, REQUIMTE, Dept Quim, 2829-516 Campus Caparica, P-2829516 Monte De Caparica, PortugalUniv Nova Lisboa, Fac Ciencias &amp; Tecnol, REQUIMTE, Dept Quim, 2829-516 Campus Caparica, P-2829516 Monte De Caparica, PortugalUniv Nova Lisboa, Fac Ciencias &amp; Tecnol, REQUIMTE, Dept Quim, P-2829516 Monte De Caparica, PortugalIIQAB CSIC, Barcelona 08024, SpainUniv Vigo, Analyt &amp; Food Chem Dept, Fac Sci, Nutr &amp; Bromatol Grp, E-32004 Orense, SpainUniv Vigo, Fac Sci, Dept Phys Chem, E-32004 Orense, Spain</style></auth-address></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aviles, T.</style></author><author><style face="normal" font="default" size="100%">Dinis, A.</style></author><author><style face="normal" font="default" size="100%">Drew, M. G. B.</style></author><author><style face="normal" font="default" size="100%">Felix, V.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A novel infinite 1-D chain of Silver(I) bridged by trans-azobenzene</style></title><secondary-title><style face="normal" font="default" size="100%">Monatshefte Fur Chemie</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Monatsh Chem</style></alt-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">binuclear</style></keyword><keyword><style  face="normal" font="default" size="100%">chemistry</style></keyword><keyword><style  face="normal" font="default" size="100%">coordination polymer</style></keyword><keyword><style  face="normal" font="default" size="100%">crystal structure</style></keyword><keyword><style  face="normal" font="default" size="100%">molecular-structures</style></keyword><keyword><style  face="normal" font="default" size="100%">molybdenum</style></keyword><keyword><style  face="normal" font="default" size="100%">networks</style></keyword><keyword><style  face="normal" font="default" size="100%">rhenium complexes</style></keyword><keyword><style  face="normal" font="default" size="100%">silver(i)</style></keyword><keyword><style  face="normal" font="default" size="100%">trans-azobenzene</style></keyword><keyword><style  face="normal" font="default" size="100%">x-ray-diffraction</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2000</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Dec</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://000166378000009</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">12</style></number><volume><style face="normal" font="default" size="100%">131</style></volume><pages><style face="normal" font="default" size="100%">1305-1310</style></pages><isbn><style face="normal" font="default" size="100%">0026-9247</style></isbn><language><style face="normal" font="default" size="100%">English</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The self-assembly of Ag[BF(4)] with trans-azobenzene in dichloromethane yields a new coordination polymer ([Ag(mu -trans-azobenzene)H(2)O] [BF(4)])(n) which was characterized by X-ray single crystal diffraction. The crystal consists of 1-D zigzag cationic chains made up from [Ag(H(2)O)](+) units linked by trans-azobenzene bridges and BF(4)(-) anions. Hydrogen bonding interactions between the chains and BF(4)(-) anions occur via intermolecular C-H . . .F and O-H . . .F contacts, and the crystal displays a 2-D supramolecular structure.&lt;/p&gt;
</style></abstract><accession-num><style face="normal" font="default" size="100%">ISI:000166378000009</style></accession-num><notes><style face="normal" font="default" size="100%">&lt;p&gt;391VYTimes Cited:1Cited References Count:22&lt;/p&gt;
</style></notes><auth-address><style face="normal" font="default" size="100%">Aviles, TUniv Nova Lisboa, Fac Ciencias &amp; Tecnol, Ctr Quim Fina &amp; Biotecnol, Dept Quim, P-2825114 Monte De Caparica, PortugalUniv Nova Lisboa, Fac Ciencias &amp; Tecnol, Ctr Quim Fina &amp; Biotecnol, Dept Quim, P-2825114 Monte De Caparica, PortugalUniv Nova Lisboa, Fac Ciencias &amp; Tecnol, Ctr Quim Fina &amp; Biotecnol, Dept Quim, P-2825114 Monte De Caparica, PortugalUniv Reading, Dept Chem, Reading RG6 2AD, Berks, EnglandUniv Aveiro, Dept Quim, P-3810193 Aveiro, Portugal</style></auth-address></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aviles, T.</style></author><author><style face="normal" font="default" size="100%">Barroso, F.</style></author><author><style face="normal" font="default" size="100%">Royo, P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">New Neutral and Cationic Cyclopentadienylcobalt Complexes</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Organometallic Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Organomet Chem</style></alt-title></titles><dates><year><style  face="normal" font="default" size="100%">1987</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jun 9</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://A1987H820000014</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">3</style></number><volume><style face="normal" font="default" size="100%">326</style></volume><pages><style face="normal" font="default" size="100%">423-429</style></pages><isbn><style face="normal" font="default" size="100%">0022-328X</style></isbn><language><style face="normal" font="default" size="100%">English</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><accession-num><style face="normal" font="default" size="100%">ISI:A1987H820000014</style></accession-num><notes><style face="normal" font="default" size="100%">&lt;p&gt;H8200Times Cited:2Cited References Count:12&lt;/p&gt;
</style></notes><auth-address><style face="normal" font="default" size="100%">Univ Alcala Henares,Dept Quim Inorgan,Alcala Henares,Spain</style></auth-address></record><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aviles, T.</style></author><author><style face="normal" font="default" size="100%">Barroso, F.</style></author><author><style face="normal" font="default" size="100%">Royo, P.</style></author><author><style face="normal" font="default" size="100%">Noordik, J. H.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">New Eta-Allyl Eta-Cyclopentadienylcobalt Cations</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Organometallic Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Organomet Chem</style></alt-title></titles><dates><year><style  face="normal" font="default" size="100%">1982</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://A1982PJ42300011</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">1</style></number><volume><style face="normal" font="default" size="100%">236</style></volume><pages><style face="normal" font="default" size="100%">101-108</style></pages><isbn><style face="normal" font="default" size="100%">0022-328X</style></isbn><language><style face="normal" font="default" size="100%">English</style></language><abstract><style face="normal" font="default" size="100%">n/a</style></abstract><accession-num><style face="normal" font="default" size="100%">ISI:A1982PJ42300011</style></accession-num><notes><style face="normal" font="default" size="100%">&lt;p&gt;Pj423Times Cited:7Cited References Count:9&lt;/p&gt;
</style></notes><auth-address><style face="normal" font="default" size="100%">Aviles, TUniv Alcala Henares,Dept Quim Inorgan,Alcala Henares,SpainUniv Alcala Henares,Dept Quim Inorgan,Alcala Henares,SpainUniv Nijmegen,Crystallog Lab,6525 Ed Nijmegen,Netherlands</style></auth-address></record></records></xml>