@article {2087,
	title = {Tricarbonyl N,N {\textquoteright},N {\textquoteright}{\textquoteright}-tris(2,6-diisopropylphenyl)guanidine molybdenum(0)},
	journal = {Acta Crystallographica Section E-Structure Reports Online},
	volume = {67},
	year = {2011},
	note = {Times Cited: 0Boere, Rene T. Masuda, Jason D.Part 7},
	month = {Jul},
	pages = {M895-U746},
	abstract = {In the title compound, [Mo(C37H53N3)(CO)(3)], the Mo atom to ring-centroid distance in the eta(6)-coordinated tricarbonyl-molybdenum group is 1.958 (1) angstrom. The three C O groups are pseudo-octahedrally disposed with C-Mo-C angles ranging from 80.7 (1) to 87.4 (1)degrees. The two uncoordinated 2,6-diisopropylphenyl-substituted benzene rings form dihedral angles of 75.96 (8) and 78.01 (9)degrees with the mean plane of the guanidine group. The coordinated benzene ring is in a slight sofa conformation with the N-substituted C atom and the bonded N atom dispaced by 0.090 (3) and 0.458 (4) angstrom, respectively, from the mean plane of the remaining ring atoms. In the crystal, despite there being two N-H donor groups, no conventional hydrogen bonds are present. This may be because of the steric effects of the bulky diisopropylphenyl groups.},
	isbn = {1600-5368},
	url = {<Go to ISI>://WOS:000294663000054},
	author = {Boer{\'e}, R. T. and Masuda, J. D.}
}
