scholarly journals Synthesis and Characterization of New Dinuclear Complexes (CO)5MnRe(CO)3(L) (L = 2,2'-Bipyrimidine, 2,3-Bis(2-pyridyl)pyrazine) and Trinuclear Compounds (CO)5MnRe(CO)3(L)R (R = Re(Br)(CO)3, W(CO)4). Evidence for Asymmetric Distortion of the Bridging 2,2'-Bipyrimidine Ligand (L) in (CO)5MnRe(CO)3(L)Re(Br)(CO)3 from the Crystal Structure and 1H-NMR and Resonance Raman Spectra

1995 ◽  
Vol 34 (19) ◽  
pp. 4756-4766 ◽  
Author(s):  
J. W. M. van Outersterp ◽  
D. J. Stufkens ◽  
J. Fraanje ◽  
K. Goubitz ◽  
A. Vlcek

1991 ◽  
Vol 3 (1) ◽  
pp. 123-127 ◽  
Author(s):  
Sara C. Huckett ◽  
Robert J. Donohoe ◽  
Laura A. Worl ◽  
Alain D. F. Bulou ◽  
Carol J. Burns ◽  
...  


1981 ◽  
Vol 20 (6) ◽  
pp. 1718-1722 ◽  
Author(s):  
Genevieve. Chottard ◽  
Pierrette. Battioni ◽  
Jean Paul. Battioni ◽  
Marc. Lange ◽  
Daniel. Mansuy


Author(s):  
B. LATTE ◽  
A. KIENAST ◽  
C. BRUHN ◽  
A. LOIDL ◽  
H. HOMBORG

The lithium phthalocyaninate(1-) iodine inclusion complex [( Lipc −)· I ], prepared by the reaction of anhydrous lithium iodide with molten 1,2-dicyanobenzene, crystallizes tetragonally in the space group P4/mcc with a = 14.057(3) Å, b = 6.397(1) Å, V = 1264.0(4) Å3, Z = 2. Lithium is in a crystallographically imposed strictly square planar coordination geometry with a Li - N distance of 1.940(7) Å. Linear chains of equidistant iodine atoms are segregated from adjacent metal-over-metal stacks of the planar lithium phthalocyaninate(1-) molecules, which are staggered by 40.2(5)°. Resonance Raman spectra have been studied in comparison with those of the starch-iodine complex [(starch)·I]. The identity of the iodine chromophore in both complexes is essentially the same. It consists of an iodine chain in a hydrophobic environment. Its character is predominately ‘aliphatic’ in [(starch)·I] and ‘aromatic’ in [( Lipc −)· I ].





1977 ◽  
Vol 48 (1) ◽  
pp. 55-58 ◽  
Author(s):  
T. Kitagawa ◽  
M. Abe ◽  
Y. Kyogoku ◽  
H. Ogoshi ◽  
H. Sugimoto ◽  
...  


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