@article { ISI:000290127500055,
	title = {Halogen bonding in 2,5-dichloro-1,4-benzoquinone: insights from experimental and theoretical charge density analysis},
	journal = {Crystal Growth \& Design},
	volume = {11},
	number = {5},
	year = {2011},
	month = {MAY},
	pages = {1855-1862},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>Experimental charge density distribution in 2, 5-dichloro-1, 4-benzoquinone has been carried out using high resolution X-ray diffraction data at 90 K to quantitatively evaluate the nature of C-Cl center dot center dot center dot O=C halogen bond in molecular crystals. Additionally, the halogen bond is studied from geometrical point of view and the same has been visualized using Hirshfeld surface analysis. The obtained results from experimental charge density analysis are compared with periodic quantum calculations using B3LYP 6-31G(d,p) level of theory. The topological values at bond critical point, three-dimensional static deformation density features and electrostatic potential isosurfaces unequivocally establish the attractive nature of C-Cl center dot center dot center dot O=C halogen bond in crystalline lattice.</p>},
	issn = {1528-7483},
	doi = {10.1021/cg2000415},
	author = {Hathwar, Venkatesha R. and Gonnade, Rajesh G. and Munshi, Parthapratim and Bhadbhade, Mohan M. and Row, Tayur N. Guru}
}
@article { ISI:000363666000023,
	title = {Highly emissive organic solids with remarkably broad color tunability based on N,C-chelate, four-coordinate organoborons},
	journal = {Chemical Communications},
	volume = {51},
	number = {89},
	year = {2015},
	month = {SEP},
	pages = {16115-16118},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>Molecular fluorophores based on N,C-chelate, four-coordinate organo-borons exhibit tunable solid-state emission colors that cover the whole visible region from blue to red. The emission color can be tuned through the substituents on either quinolines or the boron center.</p>},
	issn = {1359-7345},
	doi = {10.1039/c5cc06351e},
	author = {Shaikh, Aslam C. and Ranade, Dnyanesh S. and Thorat, Shridhar and Maity, Arunava and Kulkarni, Prasad P. and Gonnade, Rajesh G. and Munshi, Parthapratim and Patil, Nitin T.}
}
