<?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%">Arulkashmir, Arulraj</style></author><author><style face="normal" font="default" size="100%">Mahale, Rajashree Y.</style></author><author><style face="normal" font="default" size="100%">Dharmapurikar, Satej S.</style></author><author><style face="normal" font="default" size="100%">Jangid, Manoj K.</style></author><author><style face="normal" font="default" size="100%">Krishnamoorthy, Kothandam</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Supramolecular interaction facilitated small molecule films for organic field effect transistors</style></title><secondary-title><style face="normal" font="default" size="100%">Polymer Chemistry</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">APR</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">3</style></volume><pages><style face="normal" font="default" size="100%">1641-1646</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Metalloporphyrins and metal free porphyrins have been explored as active materials in field effect transistors. Amorphous forms of these porphyrins are preferred over their crystalline analogue due to the ease of solution processability. To achieve solution processability, a metalloporphyrin was anchored on a vinyl polymer by taking advantage of the supramolecular interaction between the metal and the pyridine moiety of the polymer. Non covalent bonding was preferred because it provides an opportunity to better manipulate the polymer's properties compared to its covalent bonding analogue. The binding between the porphyrin and the polymer was optimised in solution and the supramolecular complex was spun on various substrates to form thin films. The porphyrin was found to be uniformly distributed throughout the polymer films contrary to the existing approaches, wherein small molecule phase segregates in the polymer film. Field effect transistors were fabricated using the porphyrin-polymer complex and the device parameters were measured at atmospheric condition. The devices annealed at 80 degrees C showed hole carrier mobility of 2.0 x 10(-4) cm(2) V-1 s(-1) with charge trapping at the dielectric semiconductor interface. Furthermore, the high carrier mobility observed at low temperature annealing makes this supramolecular complex an attractive candidate to explore in flexible substrates.</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">5.687</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%">Dharmapurikar, Satej S.</style></author><author><style face="normal" font="default" size="100%">Arulkashmir, Arulraj</style></author><author><style face="normal" font="default" size="100%">Mahale, Rajashree Y.</style></author><author><style face="normal" font="default" size="100%">Chini, Mrinmoy Kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis of amphiphilic isoindigo co-polymers for organic field effect transistors: A comparative study</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the apllied polymer science</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Alkyl</style></keyword><keyword><style  face="normal" font="default" size="100%">Applications; Conducting polymers; Copolymers; Optical and Photovoltaic applications</style></keyword><keyword><style  face="normal" font="default" size="100%">conjugated polymers</style></keyword><keyword><style  face="normal" font="default" size="100%">High-performance</style></keyword><keyword><style  face="normal" font="default" size="100%">mobility</style></keyword><keyword><style  face="normal" font="default" size="100%">Packaging</style></keyword><keyword><style  face="normal" font="default" size="100%">Semicondoctors</style></keyword><keyword><style  face="normal" font="default" size="100%">Side-chains</style></keyword><keyword><style  face="normal" font="default" size="100%">Solar-cells</style></keyword><keyword><style  face="normal" font="default" size="100%">Thin-film Transformer</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">NOV</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">134</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;span style=&quot;color: rgb(51, 51, 51); font-family: arial, helvetica, sans-serif; font-size: 13px; background-color: rgb(248, 248, 248);&quot;&gt;In this work, the amphiphilic isoindigo (am-iInd) based conjugated polymers namely poly(am-iInd-DT) and poly(am-iInd-TT) and their regular counterpart poly(reg-iInd-DT) and poly(reg-iInd-TT) were synthesized to compare their opto-electronic and charge transport properties. They were used to fabricate organic field effect transistors. Charge transport properties in conjugated polymers depend upon intermolecular interaction which is strongly affected by the nature of side chains. The amphiphilic nature of the conjugated polymers has little impact on the charge transport properties. The charge carrier mobility of amphiphilic conjugated polymers was comparable with the regular polymers except poly(reg-iInd-DT) which can be correlated by X-ray diffraction and thin film morphology. (c) 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017, 134, 45461.&lt;/span&gt;&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">43</style></issue><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;1.866&lt;/p&gt;</style></custom4><section><style face="normal" font="default" size="100%">45461</style></section></record></records></xml>