<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shylesh, S.</style></author><author><style face="normal" font="default" size="100%">Samuel, Prinson P.</style></author><author><style face="normal" font="default" size="100%">Sisodiya, Sheetal</style></author><author><style face="normal" font="default" size="100%">Singh, A. P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Periodic mesoporous silicas and organosilicas: an overview towards catalysis</style></title><secondary-title><style face="normal" font="default" size="100%">Catalysis Surveys from Asia</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acid catalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">epoxidation</style></keyword><keyword><style  face="normal" font="default" size="100%">Mesoporous organosilicas</style></keyword><keyword><style  face="normal" font="default" size="100%">Organic-inorganic hybrid materials</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">DEC</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">4</style></number><publisher><style face="normal" font="default" size="100%">SPRINGER/PLENUM PUBLISHERS</style></publisher><pub-location><style face="normal" font="default" size="100%">233 SPRING ST, NEW YORK, NY 10013 USA</style></pub-location><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">266-282</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Micelle-templated mesoporous and organic-inorganic hybrid mesoporous materials are important in many fields of material research, especially for hosting catalysts in confined space. Among this class, the recent discovery of periodic mesoporous organosilicas (PMOs) represent an exciting new group of organic-inorganic nanocomposites targeted for a broad range of applications ranging from catalysis to microelectronics. Compared to the earlier generation of organic-inorganic hybrid mesoporous samples, obtained by the cocondensation reaction or by the grafting reaction, PMOs represent the right combination of organic and inorganic groups in the frame wall positions. This article reviews the current state of art in organic-inorganic hybrid mesoporous material research with special emphasis over periodic mesoporous organosilica materials having various redox centers (Ti, V, Cr) suitable for oxidation reactions as well as acidic sites (Al, -SO(3)H) for the organic transformation of bulky molecules.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;2.432&lt;/p&gt;</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sisodiya, Sheetal</style></author><author><style face="normal" font="default" size="100%">Shylesh, S.</style></author><author><style face="normal" font="default" size="100%">Singh, A. P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Tin incorporated periodic mesoporous organosilicas (Sn-PMOs): synthesis, characterization, and catalytic activity in the epoxidation reaction of olefins</style></title><secondary-title><style face="normal" font="default" size="100%">Catalysis Communications</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">epoxidation</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrothermal stability</style></keyword><keyword><style  face="normal" font="default" size="100%">Mesoporous</style></keyword><keyword><style  face="normal" font="default" size="100%">Organosilica</style></keyword><keyword><style  face="normal" font="default" size="100%">Sn-MCM-41</style></keyword><keyword><style  face="normal" font="default" size="100%">Sn-PMO</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style  face="normal" font="default" size="100%">MAR</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">7</style></number><publisher><style face="normal" font="default" size="100%">ELSEVIER SCIENCE BV</style></publisher><pub-location><style face="normal" font="default" size="100%">PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS</style></pub-location><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">629-633</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Tin incorporated mesoporous organosilicas (Sn-PMO) having uniform hexagonal arrangements were prepared using alkyl trimethylammonium bromide surfactants under basic reaction conditions. Characterization techniques revealed that the structural ordering, morphology, and the percentage of tin incorporation depend critically on the hydrophobic chain length of surfactants. The Sn-PMO samples are thermally stable up to 500 degrees C under air atmosphere and were hydrothermally stable up to 100 h in boiling water. The organotinsilicates showed excellent catalytic activity and reusability in the epoxidation of norbornene and ciscyclooctene than an Sn-MCM-41 due to organic groups in the frame wall positions and the better accessibility of reactants to the active sites. (C) 2010 Elsevier B.V. All rights reserved.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">7</style></issue><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">2.986
</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sisodiya, Sheetal</style></author><author><style face="normal" font="default" size="100%">Lazar, Anish</style></author><author><style face="normal" font="default" size="100%">Shylesh, Sankaranarayanapillai</style></author><author><style face="normal" font="default" size="100%">Wang, Lei</style></author><author><style face="normal" font="default" size="100%">Thiel, Werner R.</style></author><author><style face="normal" font="default" size="100%">Singh, Anand Pal</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Covalently anchored ruthenium-phosphine complex on mesoporous organosilica: catalytic applications in hydrogenation reactions</style></title><secondary-title><style face="normal" font="default" size="100%">Catalysis Communications</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Heterogenization</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrogenation</style></keyword><keyword><style  face="normal" font="default" size="100%">Organosilica</style></keyword><keyword><style  face="normal" font="default" size="100%">ruthenium</style></keyword><keyword><style  face="normal" font="default" size="100%">Triphenyl phosphine</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">AUG</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">ELSEVIER SCIENCE BV</style></publisher><pub-location><style face="normal" font="default" size="100%">PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS</style></pub-location><volume><style face="normal" font="default" size="100%">25</style></volume><pages><style face="normal" font="default" size="100%">22-27</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;New heterogeneous catalysts for alkene hydrogenation reactions were prepared by the immobilization of trimethoxysilane functionalized triphenylphosphine eta(6)-p-cymene ruthenium complex on mesoporous organosilica (PMO-Ru). Characterization techniques confirmed the structural integrity of the organosilica material and proved the successful anchoring of ruthenium complex. Catalytic activity and stability of PMO-Ru sample investigated in the hydrogenation of various olefins showed higher activity than a neat and MCM-41 supported ruthenium catalyst. High catalytic activity and stability of organosilica supported ruthenium catalyst are attributed to the hydrophobic environments and to the unique structural features imparted from the presence of organic groups in the framewall positions. (C) 2012 Elsevier B.V. All rights reserved.&lt;/p&gt;</style></abstract><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">2.915
</style></custom4></record></records></xml>