@article { ISI:000227107500022,
	title = {Synthesis, structure, electrochemistry and ROMP-activity of new ferrocenyl analog of Grubbs{\textquoteright} metathesis catalyst},
	journal = {Journal of Organometallic Chemistry},
	volume = {690},
	number = {4},
	year = {2005},
	month = {FEB},
	pages = {1018-1027},
	publisher = {ELSEVIER SCIENCE SA},
	address = {PO BOX 564, 1001 LAUSANNE, SWITZERLAND},
	abstract = {<p>Treatment of [(PCy3)(2)Cl2Ru=CH-Ph] (1) with vinylferrocene 1 and 1-ferrocenyl-1,3-butadiene 2 yielded solid products. These new complexes were characterized by H-1 NMR, P-31 NMR and C-13 NMR spectroscopy. X-ray crystal structures of both the complexes have been solved. The crystal structure of II confirmed the assigned structure and revealed existence of two sets of intermolecular C-H-Cl(M) type interactions, viz. (Ru)Cl-H-C(ferrocene) and (Ru)Cl-H-CHCl2. The air-stable, dark solid II is all efficient catalyst for ring-opening metathesis polymerization (ROMP) of cyclopentene, norbornene and cycloocta-1,5-diene. Electrochemical behavior of the complexes clearly reflects electronic communication between two metal centers. (C) 2004 Elsevier B.V. All rights reserved.</p>},
	keywords = {Electrochemistry, ferrocene, Metathesis, non-covalent interactions, ring-opening metathesis polymerization, ruthenium carbene},
	issn = {0022-328X},
	doi = {10.1016/j.jorganchem.2004.11.012},
	author = {Maishal, T. K. and Mondal, Biplab and Puranik, Vedavati G. and Wadgaonkar, P. P. and Lahiri, Goutam Kumar and Sarkar, A.}
}
@article { ISI:000378392200016,
	title = {Reductive nitrosylation of nickel(II) complex by nitric oxide followed by nitrous oxide release},
	journal = {Dalton Transactions},
	volume = {45},
	number = {25},
	year = {2016},
	month = {MAY},
	pages = {10200-10208},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>Ni(II) complex of ligand L (L = bis(2-ethyl-4-methylimidazol-5-yl)methane) in methanol solution reacts with an equivalent amount of NO resulting in a corresponding Ni(I) complex. Adding further NO equivalent affords a Ni(I)-nitrosyl intermediate with the {NiNO}(10) configuration. This nitrosyl intermediate upon subsequent reaction with additional NO results in the release of N2O and formation of a Ni(II)-nitrito complex. Crystallographic characterization of the nitrito complex revealed a symmetric eta(2)-O,O-nitrito bonding to the metal ion. This study demonstrates the reductive nitrosylation of a Ni(II) center followed by N2O release in the presence of excess NO.</p>},
	issn = {1477-9226},
	doi = {10.1039/c6dt00826g},
	author = {Ghosh, Somnath and Deka, Hemanta and Dangat, Yuvraj B. and Saha, Soumen and Gogoi, Kuldeep and Vanka, Kumar and Mondal, Biplab}
}
