Reactions of Iridium and Rhodium Complexes Containing η2-Benzyne, η2-Tetrafluorobenzyne, and η2-Trifluorobenzyne Ligands. Differential Rates of Arene Elimination by Protonation of Isomeric Fluoroaryl Complexes and Restricted Rotation of PMe3Ligands inortho-Iodo andortho-Bromoaryl Complexes

2003 ◽  
Vol 22 (10) ◽  
pp. 2134-2141 ◽  
Author(s):  
Russell P. Hughes ◽  
Roman B. Laritchev ◽  
Alex Williamson ◽  
Christopher D. Incarvito ◽  
Lev N. Zakharov ◽  
...  
1990 ◽  
Vol 55 (4) ◽  
pp. 1106-1111 ◽  
Author(s):  
John Matsoukas ◽  
Paul Cordopatis ◽  
Raghav Yamdagni ◽  
Graham J. Moore

The conformational properties of the Sarmesin analogues [N-MeAib1, Tyr(Me)4]ANGII and [N-MeAib1, Tyr(Me)4, Ile8]ANGII in hexadeutero-dimethysulfoxide were investigated by Nuclear Overhauser Effect (NOE) Enhancement Studies. Cis-trans isomers (ratio 1 : 6) due to restricted rotation of the His-Pro bond were observed. Interresidue interactions between the His Cα proton and the two Pro Cδ protons revealed that the major isomer was the trans.


2006 ◽  
Vol 71 (2) ◽  
pp. 197-206 ◽  
Author(s):  
Martin Pošta ◽  
Jan Čermák ◽  
Pavel Vojtíšek ◽  
Ivana Císařová

The first rhodium complexes of diphosphinoazines [{RhCl(1,2-η:5,6-η-CH=CHCH2CH2CH=CHCH2CH2)}2 {μ-R2PCH2C(But)=NN=C(But)CH2PR2] (R = Ph, Cy, Pri) were prepared by cleavage of the bridge in chloro(cycloocta-1,5-diene)rhodium(I) dimer, the analogous iridium(I) complexes were also prepared for the first time. The X-ray structures of isostructural rhodium and iridium complexes with bis(dicyclohexylphosphino)pinacoloneazine were determined. Diphosphinoazine ligands in the complexes remained in (Z,Z) configuration bridging two RhCl(C8H12) units.


RSC Advances ◽  
2019 ◽  
Vol 9 (50) ◽  
pp. 29396-29404 ◽  
Author(s):  
Magdalena Jankowska-Wajda ◽  
Olga Bartlewicz ◽  
Andrea Szpecht ◽  
Adrian Zajac ◽  
Marcin Smiglak ◽  
...  

Platinum and rhodium complexes ligated by imidazolium substituted phosphine were obtained with high yields and applied as efficient catalysts.


1976 ◽  
Vol 31 (8) ◽  
pp. 1017-1018 ◽  
Author(s):  
H. Oehling ◽  
F. Baer

Abstract Polymethine oxonols show temperature dependent 1H-NMR-spectra because of restricted rotation of the end groups. The dependence of the value of the corresponding free enthalpy of activation AGt on the length of the poly-methine chain can be explained by the change of the π-electron contribution to ⊿G≠.


Sign in / Sign up

Export Citation Format

Share Document