<?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%">Sengupta, J.</style></author><author><style face="normal" font="default" size="100%">Mukhopadhyay, R.</style></author><author><style face="normal" font="default" size="100%">Bhattacharjya, A.</style></author><author><style face="normal" font="default" size="100%">Bhadbhade, Mohan M.</style></author><author><style face="normal" font="default" size="100%">Bhosekar, Gaurav V.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and intramolecular nitrile oxide cycloaddition of 3,5 `-ether-linked pseudooligosaccharide derivatives: an approach to chiral macrooxacycles</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Organic Chemistry</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style  face="normal" font="default" size="100%">OCT</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">21</style></number><publisher><style face="normal" font="default" size="100%">AMER CHEMICAL SOC</style></publisher><pub-location><style face="normal" font="default" size="100%">1155 16TH ST, NW, WASHINGTON, DC 20036 USA</style></pub-location><volume><style face="normal" font="default" size="100%">70</style></volume><pages><style face="normal" font="default" size="100%">8579-8582</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;[GRAPHIC] 3,5'-Ether-linked pseudooligopentose derivatives were synthesized for the first time from readily available carbohydrate precursors. The 1,2-isopropylidene-protected ether-linked oligopentoses are potentially important as precursors of novel RNA analogues. Intramolecular cycloaddition of the nitrile oxides prepared from these derivatives led to the diastereoselective formation of chiral isoxazolines fused to 10-16-membered oxacycles. The stereochemistry of some of these isoxazolines was established by X-ray diffraction and NOESY analysis.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">21</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">4.785</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%">Ray, A.</style></author><author><style face="normal" font="default" size="100%">Manoj, Kochunnoonny</style></author><author><style face="normal" font="default" size="100%">Bhadbhade, Mohan M.</style></author><author><style face="normal" font="default" size="100%">Mukhopadhyay, R.</style></author><author><style face="normal" font="default" size="100%">Bhattacharjya, A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cu(I)-catalyzed cycloaddition of constrained azido-alkynes: access to 12- to 17-membered monomeric triazolophanes incorporating furanoside rings</style></title><secondary-title><style face="normal" font="default" size="100%">Tetrahedron Letters</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2006</style></year><pub-dates><date><style  face="normal" font="default" size="100%">APR</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">16</style></number><publisher><style face="normal" font="default" size="100%">PERGAMON-ELSEVIER SCIENCE LTD</style></publisher><pub-location><style face="normal" font="default" size="100%">THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND</style></pub-location><volume><style face="normal" font="default" size="100%">47</style></volume><pages><style face="normal" font="default" size="100%">2775-2778</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;A strained monomeric 12-membered triazolophane was formed by the Cu(I)-catalyzed intramolecular cycloaddition of an azide to an alkyne having a constrained tether incorporating ail aromatic ring and a furanoside ring. Similar cycloadditions of azido-alkynes having ester, furanoside and peptidic tethers led to the formation of monomeric triazolophanes of higher ring sizes. (c) 2006 Elsevier Ltd. All rights reserved.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">16</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><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%">2.347</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jijil, Chamundi P.</style></author><author><style face="normal" font="default" size="100%">Rajarajan, A. K.</style></author><author><style face="normal" font="default" size="100%">Devi, R. Nandini</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mittal, R.</style></author><author><style face="normal" font="default" size="100%">Chauhan, A. K.</style></author><author><style face="normal" font="default" size="100%">Mukhopadhyay, R.</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Noble metal ions incorporated in lattice points of perovskites - water gas shift activity of BaCe1-xPtxO3-d</style></title><secondary-title><style face="normal" font="default" size="100%">56th DAE-Solid State Physics Symposium (SSPS)</style></secondary-title><tertiary-title><style face="normal" font="default" size="100%">AIP Conference Proceedings</style></tertiary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">BaCeO3</style></keyword><keyword><style  face="normal" font="default" size="100%">Neutron diffraction</style></keyword><keyword><style  face="normal" font="default" size="100%">Platinum catalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">WGS reaction</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%">JUN</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Govt India, Dept Atom Energy (DAE), Board Res Nucl Sci (BRNS)</style></publisher><pub-location><style face="normal" font="default" size="100%">2 Huntington Quadrangle, Ste 1no1, Melville, NY 11747-4501 USA</style></pub-location><volume><style face="normal" font="default" size="100%">1447</style></volume><pages><style face="normal" font="default" size="100%">1277-1278</style></pages><isbn><style face="normal" font="default" size="100%">978-0-7354-1044-2</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Recently precious metals supported on oxides were reported to be very promising catalysts for the lower-temperature WGS reaction. Here we report the synthesis of platinum doped barium cerate and its use as catalysts for WGS reaction. It has been found that maximum CO conversion was obtained at 350 degrees C which enhanced after the first cycle. XPS analysis shows that after the first cycle more ionic Platinum species are present on the surface of the catalyst. Neutron diffraction at room temperature shows that the oxygen vacancies are in the O2 position and increases with increasing Pt substitution.&lt;/p&gt;</style></abstract><notes><style face="normal" font="default" size="100%">56th DAE-Solid State Physics Symposium (SSPS), SRM Univ, Kattankulathur, INDIA, DEC 19-23, 2011</style></notes></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%">Samui, Barun Kumar</style></author><author><style face="normal" font="default" size="100%">Prakasan, Manikanda Priya</style></author><author><style face="normal" font="default" size="100%">Ramesh, C.</style></author><author><style face="normal" font="default" size="100%">Chakrabarty, Debabrata</style></author><author><style face="normal" font="default" size="100%">Mukhopadhyay, R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Structure-property relationship of different types of polyester industrial yarns</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the Textile Institute</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">modulus</style></keyword><keyword><style  face="normal" font="default" size="100%">orientation</style></keyword><keyword><style  face="normal" font="default" size="100%">polyester</style></keyword><keyword><style  face="normal" font="default" size="100%">shrinkage</style></keyword><keyword><style  face="normal" font="default" size="100%">structure</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style  face="normal" font="default" size="100%">JAN</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">1</style></number><publisher><style face="normal" font="default" size="100%">TAYLOR &amp; FRANCIS LTD</style></publisher><pub-location><style face="normal" font="default" size="100%">4 PARK SQUARE, MILTON PARK, ABINGDON OX14 4RN, OXON, ENGLAND</style></pub-location><volume><style face="normal" font="default" size="100%">104</style></volume><pages><style face="normal" font="default" size="100%">35-45</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Four major types of polyester industrial yarns (1000 Denier) which are used commercially were studied for their key structural parameters. An attempt has been made to establish a relationship between morphology and properties of these yarns. High tenacity (HT) polyester yarn has the highest birefringence, amorphous orientation, and long period but is relatively less crystalline. High shrinkage characteristic of HT polyester yarn can be accounted for its higher amorphous orientation. High modulus low shrinkage (HMLS) polyester yarn has higher crystallinity and crystal size compared to HT yarn. Fraction of tie molecules of these yarns has been calculated and found that low shrinkage (LS) and super low shrinkage (SLS) yarns have lesser tie molecules. These LS and SLS yarns are tailor-made to achieve lower shrinkage and at the same time maintaining a good level of tenacity. This is achieved with lower amorphous orientation in the final drawn yarn structure. Amorphous orientation was found to have stronger influence than any other structural parameter on the key yarn properties like modulus, tenacity, elongation, and shrinkage.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">0.77
</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%">Samui, Barun Kumar</style></author><author><style face="normal" font="default" size="100%">Dasgupta, Saikat</style></author><author><style face="normal" font="default" size="100%">Mukhopadhyay, R.</style></author><author><style face="normal" font="default" size="100%">Ramesh, C.</style></author><author><style face="normal" font="default" size="100%">Chakrabarty, Debabrata</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Studies on the static and dynamic properties of different types of polyester industrial yarns</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the Textile Institute</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">creep</style></keyword><keyword><style  face="normal" font="default" size="100%">modulus</style></keyword><keyword><style  face="normal" font="default" size="100%">polyester</style></keyword><keyword><style  face="normal" font="default" size="100%">shrinkage</style></keyword><keyword><style  face="normal" font="default" size="100%">tan delta</style></keyword><keyword><style  face="normal" font="default" size="100%">work loss</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">OCT</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">9</style></number><publisher><style face="normal" font="default" size="100%">TAYLOR &amp; FRANCIS LTD</style></publisher><pub-location><style face="normal" font="default" size="100%">2-4 PARK SQUARE, MILTON PARK, ABINGDON OR14 4RN, OXON, ENGLAND</style></pub-location><volume><style face="normal" font="default" size="100%">107</style></volume><pages><style face="normal" font="default" size="100%">1175-1184</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Four major types of polyester industrial yarns, viz. high tenacity (HT), high modulus low shrinkage (HMLS), low shrinkage (LS) and super low shrinkage (SLS) polyester yarns, were studied for their static and dynamic properties. An attempt has been made to establish a linkage between static and dynamic properties of these yarns with its structure and with its end applications. HMLS and HT polyester yarns have lower tan delta and work loss, which are the desired characteristics required for its end applications which include tire and conveyer belt. Higher overall orientation and higher fraction of tie molecules helped to achieve these properties in HT and HMLS polyester yarns. LS and SLS polyester yarns are mostly used for static applications. Low thermal shrinkage is the key requirement for the downstream processes of these yarns. Lower amorphous orientation in these two yarns is primarily responsible for achieving very low thermal shrinkage. A good co-relation has been established between the peak temperature of work loss (in slow speed hysteresis test) and the peak temperature of tan delta (in high-speed dynamic test).&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">9</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%">1.128</style></custom4></record></records></xml>