<?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%">Shaikh, Aslam C.</style></author><author><style face="normal" font="default" size="100%">Shalini, S.</style></author><author><style face="normal" font="default" size="100%">Vaidhyanathan, Ramanathan</style></author><author><style face="normal" font="default" size="100%">Mane, Manoj V.</style></author><author><style face="normal" font="default" size="100%">Barui, Ayan Kumar</style></author><author><style face="normal" font="default" size="100%">Patra, Chitta Ranjan</style></author><author><style face="normal" font="default" size="100%">Venkatesh, Yeduru</style></author><author><style face="normal" font="default" size="100%">Bangal, Prakriti Ranjan</style></author><author><style face="normal" font="default" size="100%">Patil, Nitin T.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Identifying solid luminogens through gold-catalysed intramolecular hydroarylation of alkynes</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Organic Chemistry</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cell imaging</style></keyword><keyword><style  face="normal" font="default" size="100%">Dyes/pigments</style></keyword><keyword><style  face="normal" font="default" size="100%">fluorescence</style></keyword><keyword><style  face="normal" font="default" size="100%">Gold</style></keyword><keyword><style  face="normal" font="default" size="100%">Luminescence</style></keyword><keyword><style  face="normal" font="default" size="100%">Solvatochromism</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">AUG</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">22</style></number><publisher><style face="normal" font="default" size="100%">WILEY-V C H VERLAG GMBH</style></publisher><pub-location><style face="normal" font="default" size="100%">POSTFACH 101161, 69451 WEINHEIM, GERMANY</style></pub-location><pages><style face="normal" font="default" size="100%">4860-4867</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The identification of a new class of luminogens based on pyrrolo-quinoxaline embedded coumarin (PQC) structures is reported. The reaction relies on the gold-catalyzed hydroarylation reaction of appropriately substituted aryl alkynoates that produces molecules that exhibit solvatochromism and aggregation-induced emission enhancement (AIEE) phenomena. The application of PQCs for live cell imaging has also been demonstrated.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">22</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%">3.068</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%">Haldar, Sattwick</style></author><author><style face="normal" font="default" size="100%">Rase, Deepak</style></author><author><style face="normal" font="default" size="100%">Shekhar, Pragalbh</style></author><author><style face="normal" font="default" size="100%">Jain, Chitvan</style></author><author><style face="normal" font="default" size="100%">Vinod, Chathakudath Prabhakaran</style></author><author><style face="normal" font="default" size="100%">Zhang, En</style></author><author><style face="normal" font="default" size="100%">Shupletsov, Leonid</style></author><author><style face="normal" font="default" size="100%">Kaskel, Stefan</style></author><author><style face="normal" font="default" size="100%">Vaidhyanathan, Ramanathan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Incorporating conducting polypyrrole into a polyimide COF for carbon-free ultra-high energy supercapacitor</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Energy Materials</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">carbon free capacitors</style></keyword><keyword><style  face="normal" font="default" size="100%">cation-anion co-storage</style></keyword><keyword><style  face="normal" font="default" size="100%">conductivity</style></keyword><keyword><style  face="normal" font="default" size="100%">high energy capacitors</style></keyword><keyword><style  face="normal" font="default" size="100%">polypyrrole doped COFs</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">SEP</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">2200754</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	Redox-active covalent organic frameworks (COFs) store charges but possess inadequate electronic conductivity. Their capacitive action works by storing H+ ions in an acidic electrolyte and is typically confined to a small voltage window (0-1 V). Increasing this window means higher energy and power density, but this risks COF stability. Advantageously, COF's large pores allow the storage of polarizable bulky ions under a wider voltage thus reaching higher energy density. Here, a COF-electrode-electrolyte system operating at a high voltage regime without any conducting carbon or redox active oxides is presented. Conducting polypyrrole (Ppy) chains are synthesized within a polyimide COF to gain electronic conductivity (approximate to 10 000-fold). A carbon-free quasi-solid-state capacitor assembled using this composite showcases high pseudo-capacitance (358 mF cm(-2)@1 mA cm(-2)) in an aqueous gel electrolyte. The synergy among the redox-active polyimide COF, polypyrrole and organic electrolytes allows a wide-voltage window (0-2.5 V) leading to high energy (145 mu Wh cm(-2)) and power densities (4509 mu W cm(-2)). Amalgamating the polyimide-COF and the polypyrrole as one material minimizes the charge and mass transport resistances. Computation and experiments reveal that even a partial translation of the modules/monomers intrinsic electronics to the COF imparts excellent electrochemical activity. The findings unveil COF-confined polymers as carbon-free energy storage materials.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">34</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%">&lt;p&gt;
	29.698&lt;/p&gt;
</style></custom4></record></records></xml>