ChemInform Abstract: DERIVATIVES OF DITHIOCARBAZIC ACID AS LIGANDS IN CARBONYL COMPLEXES OF MANGANESE(I) AND RHENIUM(I). THE CRYSTAL STRUCTURES OF TRICARBONYLBIS(S-METHYLDITHIOCARBAZATO)MANGANESE(I) BROMIDE AND BIS-μ-(N-ISOPROPYLIDENE-S-METHYLDITHIOCARBAZ

1980 ◽  
Vol 11 (49) ◽  
Author(s):  
H. WEBER ◽  
R. MATTES
Chemistry ◽  
2021 ◽  
Vol 3 (1) ◽  
pp. 199-227
Author(s):  
Young Hoon Lee ◽  
Jee Young Kim ◽  
Sotaro Kusumoto ◽  
Hitomi Ohmagari ◽  
Miki Hasegawa ◽  
...  

Analysis of the weak interactions within the crystal structures of 33 complexes of various 4′-aromatic derivatives of 2,2′:6′,2″-terpyridine (tpy) shows that interactions that exceed dispersion are dominated, as expected, by cation⋯anion contacts but are associated with both ligand–ligand and ligand–solvent contacts, sometimes multicentred, in generally complicated arrays, probably largely determined by dispersion interactions between stacked aromatic units. With V(V) as the coordinating cation, there is evidence that the polarisation of the ligand results in an interaction exceeding dispersion at a carbon bound to nitrogen with oxygen or fluorine, an interaction unseen in the structures of M(II) (M = Fe, Co, Ni, Cu, Zn, Ru and Cd) complexes, except when 1,2,3-trimethoxyphenyl substituents are present in the 4′-tpy.


1977 ◽  
Vol 32 (11) ◽  
pp. 1217-1221 ◽  
Author(s):  
Helmut Behrens ◽  
Rolf Hüller ◽  
Anton Jungbauer ◽  
Peter Merbach ◽  
Matthias Moll

The following known and novel cobalt carbonyl complexes are formed by reactions of cobalt metal with bipy, phen, Ph2P-CH2-CH2-PPh2 (P͡P), PPh3, Ph2P-CH2-CH2-NEt2 (P͡N), InCl, SnX2 (X = Cl, Br, I), Cd and HgBr2 under CO pressure (200 bar):[Co(bipy)3][Co(CO)4]2, [Co(phen)3][Co(CO)4]2, [Co2(P͡P)3(CO)4][Co(CO)4]2; Co2(CO)6 (PPh3)2, Co2(CO)6 (P͡N)2; [Co(CO)4]2SnCl2, {[Co(CO)4]2InCl}2; [Co(CO)3PPh3]2SnX2(X = Cl, Br, I), [Co(CO)3(P͡N)]2SnCl2, [Co(CO)3(P͡N)]2M (M = Cd, Hg).


2005 ◽  
Vol 58 (7) ◽  
pp. 531
Author(s):  
Laura Andrau ◽  
Jonathan M. White

Low-temperature X-ray crystal structures were determined on a range of derivatives of 4-thiacyclohexanol 5a of varying electron demand with a view to finding evidence for a through-bond interaction between the sulfur lone pair and the oxygenated substituent. In contrast to earlier suggestions, plots of C–OR bond distance versus pKa (ROH) showed that any interaction between the sulfur and the OR group is unlikely to be of a through-bond origin. Furthermore, unimolecular solvolysis rate measurements on the nosylate ester derivative 5g showed that the sulfur actually retards the reaction slightly in comparison with the corresponding sulfur-free analogue 6.


2014 ◽  
Vol 67 (1) ◽  
pp. 64-71 ◽  
Author(s):  
Zhihong Ma ◽  
Kaiming Guo ◽  
Na Wang ◽  
Hong Wang ◽  
Zhangang Han ◽  
...  

Tetrahedron ◽  
2015 ◽  
Vol 71 (24) ◽  
pp. 4163-4173 ◽  
Author(s):  
Alicja Kaźmierska ◽  
Marlena Gryl ◽  
Katarzyna Stadnicka ◽  
Lesław Sieroń ◽  
Andrzej Eilmes ◽  
...  

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