<?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%">Kumar, M. Naveen</style></author><author><style face="normal" font="default" size="100%">Lyngkhoi, Deikrisha Lyngdoh</style></author><author><style face="normal" font="default" size="100%">Gaikwad, Sudhakar</style></author><author><style face="normal" font="default" size="100%">Samanta, Debabrata</style></author><author><style face="normal" font="default" size="100%">Khatua, Snehadrinarayan</style></author><author><style face="normal" font="default" size="100%">Pramanik, Susnata</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The effect of substituents on the aggregation-induced emission of 9,10-phenanthraquinone-hydrazones</style></title><secondary-title><style face="normal" font="default" size="100%">New Journal of Chemistry</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">AUG </style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">47</style></volume><pages><style face="normal" font="default" size="100%">15066-15075</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	Organic luminophores, particularly &amp;amp; pi;-conjugated systems, have become crucial in modern optoelectronic devices that utilise luminescence as an output signal, requiring aggregate or solid-states, such as nanoparticles, thin films, or crystals. Herein, we report the one-step synthesis of six hydrazone derivatives using condensation reactions between 9,10-phenanthrenedione and different aromatic hydrazines, comprising electron-donating/electron-withdrawing groups and a quinoline moiety. The introduction of a conjugated &amp;amp; pi;-system leads to complete co-planarization of molecules resulting in large bathochromic shifts in their absorption profile, the maximum red-shifts ever observed for the hydrazones. These hydrazones are weakly fluorescent in dilute acetonitrile solutions. However, they exhibit enhanced emissions of up to 300-fold in aggregated states. Dynamic light scattering (DLS) and scanning electron microscopy (SEM) studies support nanoaggregate formation. All the compounds exhibit red to NIR emissions in their crystalline state with as high as 75% quantum efficiency.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">32</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;
	3.3&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%">Kumar, M. Naveen</style></author><author><style face="normal" font="default" size="100%">Lyngkhoi, Deikrisha Lyngdoh</style></author><author><style face="normal" font="default" size="100%">Gaikwad, Sudhakar</style></author><author><style face="normal" font="default" size="100%">Samanta, Jayanta</style></author><author><style face="normal" font="default" size="100%">Ahamed, Rafiq</style></author><author><style face="normal" font="default" size="100%">Khatua, Snehadrinarayan</style></author><author><style face="normal" font="default" size="100%">Pramanik, Susnata</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Excitation wavelength-dependent multi-coloured and white-light emissive pyrene-based hydrazones: suppression of Kasha's rule</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Communications</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2023</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%">59</style></volume><pages><style face="normal" font="default" size="100%">14122-14125</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	Multi-coloured and white-light emissions from pyrene-based hydrazones are described. They exhibit excitation wavelength-dependent emissions in solution due to the suppression of Kasha's rule. Interestingly, in dimethylformamide, 1-3 emit light that covers all the regions of primary colours as a function of excitation wavelength, and 1 and 2 emit white light (lambda ex = 420 nm) in isopropanol. Multi-coloured and white-light emissions from pyrene-based hydrazones are described.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">95</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;
	4.9&lt;/p&gt;
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