NMR Studies of Hindered Rotation in Cubic KCN

1968 ◽  
Vol 49 (10) ◽  
pp. 4721-4722 ◽  
Author(s):  
Eiichi Fukushima
1992 ◽  
Vol 30 (12) ◽  
pp. 1178-1185 ◽  
Author(s):  
Th. Lippert ◽  
A. Wokaun ◽  
J. Dauth ◽  
O. Nuyken

1993 ◽  
Vol 26 (1) ◽  
pp. 79-101 ◽  
Author(s):  
Laurine A. LaPlanche ◽  
Yangdong Xu ◽  
Ronnie Benshafrut ◽  
Robert Rothchild ◽  
Ernest A. Harrison

1997 ◽  
Vol 30 (8) ◽  
pp. 1669-1683 ◽  
Author(s):  
Azizeh Elias ◽  
Teresa Gail Roberts ◽  
Kunisi S. Venkatasubban ◽  
R. Rothchild

1996 ◽  
Vol 74 (11) ◽  
pp. 1936-1944
Author(s):  
Kenzo Ohkita ◽  
Hideo Asano ◽  
Hideo Kurosawa ◽  
Toshikazu Hirao ◽  
Yohko Miyaji ◽  
...  

Complexes of (η5-cyclopentadienyl)(bis(di-p-tolylphosphino)ethane)ruthenium(II) cation with some styrenes containing meta or para substituants were prepared and their NMR spectra examined in detail. Variable-temperature NMR studies on the unsubstituted and para-substituted styrene analogues demonstrated occurrence of a restricted rotation about the C(sp2)—C(sp2) single bond of the styrenes where one of the ortho hydrogens of the styrene phenyl group receives a very large diamagnetic shielding effect by one of the phosphine tolyl groups. Similar studies on the meta-substituted styrene complexes showed existence of two unequally populated conformational isomers arising from the similar restricted rotation where the meta substituent in the dominant isomer was placed further away from the C=C group. The origin of such conformational isomerism was deduced to be the buttressing effect of the meta substituent transmitted via the ortho-hydrogen atom. Key words: buttressing effect, hindered rotation, Ru–styrene complex.


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