@article { ISI:000273100600003,
	title = {Selective binding of benzoquinone with a Pt-II-cyclophane constructed on the skeleton of N,N {\textquoteleft}-bis(salicylidene)-p-phenylenediamine: synthesis and spectroscopic studies},
	journal = {Indian Journal of Chemistry Section A-Inorganic Bio-Inorganic Physical Theoretical \& Analytical Chemistry},
	volume = {48},
	number = {12},
	year = {2009},
	month = {DEC},
	pages = {1644-1651},
	publisher = {NATL INST SCIENCE COMMUNICATION-NISCAIR},
	address = {DR K S KRISHNAN MARG, PUSA CAMPUS, NEW DELHI 110 012, INDIA},
	abstract = {<p>The Schiff base NN{\textquoteright}-bis(salicylidene)-p-phenylenediamine has been complexed with Pt(en)Cl-2 and the resulting Pt-II-cyclophane, [Pt(en)L](2)center dot 4PF(6), reacted with phenol, resorcinol, hydroquinone or benzoquinone in DMSO solution. Their binding has been monitored by the variation in the corresponding UV-visible and emission spectral patterns. The binding properties are compared with the earlier reported Zn-II-cyclophane [Zn(bpy)L](2) (bpy = 2,2{\textquoteright}-bipyridine). A few solid adducts of phenol and benzoquinone with the Pt-II-cyclophane complex and hydroquinone as well as that of resorcinol with the Zn-cyclophane have also been synthesized and characterized.</p>},
	keywords = {Coordination chemistry, Cyclophanes, Metallocyclophanes, platinum, Schiff bases},
	issn = {0376-4710},
	author = {Kumari, Niraj and Prajapati, Rishikesh and Dixit, Mudit and Mishra, Lallan}
}
@article { ISI:000307748700004,
	title = {Scandium-decorated MOF-5 as potential candidates for room-temperature hydrogen storage: a solution for the clustering problem in MOFs},
	journal = {Journal of Physical Chemistry C},
	volume = {116},
	number = {33},
	year = {2012},
	month = {AUG},
	pages = {17336-17342},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>Transition-metal-based systems show promising binding energy for hydrogen storage but suffer from clustering problem. The effect of light transition metal (M = Sc, Ti) decoration, boron substitution on the hydrogen storage properties of MOF-5, and clustering problem of metals has been investigated using ab initio density, functional theory. Our results of solid-tate calculations reveal that whereas Ti clusters strongly Sc atoms do not suffer from this problem when decorating MOF-5. Boron substitution on metal-decorated MOF-5 enhances the interaction energy of both the metals with MOF-5. Sc-decorated MOF-5 shows a hydrogen storage capacity of 5.81 wt \% with calculated binding energies of 20-40 kJ/mol, which ensures the room-teniperature applicability of this hydrogen storage material.</p>},
	issn = {1932-7447},
	doi = {10.1021/jp302852h},
	author = {Dixit, Mudit and Maark, Tuhina Adit and Ghatak, Kamalika and Ahuja, Rajiv and Pal, Sourav}
}
