Welcome to Organic Materials Group
Publications (2016)
Jadhav, Bahusaheb Dhokale, Yuvraj Patil, S. M. Mobin, Rajneesh Misra*, Multi-Stimuli Responsive Donor–Acceptor Tetraphenylethylene Substituted Benzothiadiazoles,J. Phys. Chem. C2016, 120, 24030–24040. https://doi.org/10.1021/acs.jpcc.6b09015
Bahusaheb Dhokale, Thaksen Jadhav, S. M. Mobin, Rajneesh Misra*, Tetracyanobutadiene functionalized ferrocenyl BODIPY dyes, Dalton Trans. 2016, 45, 1476–1483.
T. S. Reddy, Ramesh Maragani, Rajneesh Misra*, Triarylborane substituted naphthalimide as a fluoride and cyanide ion sensor, Dalton Trans. 2016, 45, 2549–2553.
Ramesh Maragani, Prabhat Gautam, S. M. Mobin, RajneeshMisra*, C2-Symmetric ferrocenylbisthiazoles: synthesis, photophysical, electrochemical and DFT studies, Dalton Trans. 2016, 45, 4802–4809.
Bahusaheb Dhokale, Thaksen Jadhav, Yuvraj Patil, RajneeshMisra*, Symmetrical and unsymmetrical ferrocenylperylenediimides: Design, synthesis and properties. Dyes Pigm. 2016, 134, 164–170.
Yuvraj Patil, Thaksen Jadhav, Bahusaheb Dhokale, Rajneesh Misra*, Design and Synthesis of Low HOMO–LUMO Gap N-Phenylcarbazole-Substituted Diketopyrrolopyrroles, Asian J. Org. Chem. 2016, 5, 1008–1014.
T. S. Reddy, Ramesh Maragani, Bahusaheb Dhokale, S. M. Mobin, Rajneesh Misra*, Heteroatom-connected ferrocenyl substituted naphthalimides, RSC Adv. 2016, 6, 7746–7754.
Yuvraj Patil, Thaksen Jadhav, Bahusaheb Dhokale, Rajneesh Misra*, Tuning of the HOMO–LUMO Gap of Symmetrical and Unsymmetrical Ferrocenyl-Substituted Diketopyrrolopyrroles, Eur. J. Org. Chem. 2016, 733–738.
Ramesh Maragani, T.S. Reddy, Rajneesh Misra*, CS-symmetric triarylborane substituted bisthiazole for selective detection of F− and CN− ions, Tetrahedron Lett. 2016, 57, 3853–3857.
Rekha Sharma, Ramesh Maragani, RajneeshMisra*, Ferrocenylaza-dipyrromethene and aza-BODIPY: Synthesis and properties, J. Organomet. Chem. 2016, 825, 8–14.
Yuvraj Patil, Rajneesh Misra*, M. L. Keshtov, G. D. Sharma, 1,1,4,4-Tetracyanobuta-1,3-diene Substituted Diketopyrrolopyrroles: An Acceptor for Solution Processable Organic Bulk Heterojunction Solar Cells, J. Phys. Chem. C2016,120, 6324–6335.
Thaksen Jadhav, J. M. Choi, Bahusaheb Dhokale, S. M. Mobin, J. Y. Lee, Rajneesh Misra*, Effect of End Groups on Mechanochromism and Electroluminescence in Tetraphenylethylene Substituted Phenanthroimidazoles, J. Phys. Chem. C2016, 120,18487–18495.
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Prabhat Gautam, Rajneesh Misra*, G. D. Sharma, Dicyanoquinodimethane-substituted benzothiadiazole for efficient small-molecule solar cells, Phys. Chem. Chem. Phys. 2016, 18, 7235–7241.
Prabhat Gautam, Rajneesh Misra*, S. Biswas, G. D. Sharma, A D–π–A1–π–A2 push–pull small molecule donor for solution processed bulk heterojunction organic solar cells, Phys. Chem. Chem. Phys. 2016, 18, 13918–13926.
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Yuvraj Patil, Rajneesh Misra*, F. C. Chen, G. D. Sharma, Small molecule based N-phenyl carbazole substituted diketopyrrolopyrroles as donors for solution-processed bulk heterojunction organic solar cells,Phys. Chem. Chem. Phys. 2016, 18, 22999–23005
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Yuvraj Patil, Rajneesh Misra*, A. Sharma, G. D. Sharma, D–A–D–π–D–A–D type diketopyrrolopyrrole based small molecule electron donors for bulk heterojunction organic solar cell, Phys. Chem. Chem. Phys. 2016, 18, 16950–16957.
Rajneesh Misra*, Ramesh Maragani, C. P. Singh, R. Chari, Photonic properties of star shaped ferrocenyl substituted triazines, Dyes Pigm. 2016, 126, 110–117.
Rajneesh Misra*, Ramesh Maragani, D. Arora, A. Sharma, G. D. Sharma, Positional isomers of pyridine linked triphenylamine-based donor-acceptor organic dyes for efficient dye-sensitized solar cells, Dyes Pigm. 2016, 126, 38–45.
Thaksen Jadhav, J. M. Choi, J. Y. Lee, Bahusaheb Dhokale, Rajneesh Misra*, Non-doped blue organic light emitting devices based on tetraphenylethylene-π-imidazole derivatives, Organic Electronics2016, 37, 448–452.
Yuvraj Patil, Rajneesh Misra*, F. C. Chen, M. L. Keshtov, G. D. Sharma, Symmetrical and unsymmetrical triphenylamine based diketopyrrolopyrroles and their use as donors for solution processed bulk heterojunction organic solar cells, RSC Adv. 2016, 6, 99685–99694.
