Cyclopentadienyl-ruthenium and -osmium chemistry. XII. Some complexes containing cyclic carbene ligands

1980 ◽  
Vol 33 (12) ◽  
pp. 2605 ◽  
Author(s):  
MI Bruce ◽  
AG Swincer ◽  
BJ Thompson ◽  
RC Wallis

Reactions between ω-hydroxyalk-1-ynes, HC2(CH2)nOH (n = 2 or 3) or HC2CH2CHMeOH, and MX(PR3)2(η-C5H5) (M = Ru, X = Cl, R = Me or Ph; M = Os, X = Br, R = Ph) in the presence of NH4PF6 give cationic cyclic carbene complexes, presumably by rapid intramolecular cyclization of (undetected) intermediate ω-hydroxyvinylidene complexes. Further reactions of {Ru[C(CH2)3O]-(PPh3)2(η-C5H5)}+ include (a) base-catalysed H- D exchange of both H atoms of the β-CH2 group; (b) metallation and subsequent dimethylation of the β-CH2 group; (c) reduction by NaAlH2- (OCH2CH2OMe)2 to Ru[CH(CH2)3O](PPh3)2(η-C5H5).

1999 ◽  
Vol 54 (11) ◽  
pp. 1350-1356 ◽  
Author(s):  
Anthony J. Arduengo ◽  
Jens R. Goerlicha ◽  
Fredric Davidson ◽  
William J. Marshall

The first examples of carbene-cadmium complexes are reported from the reactions of a variety of imidazol-2-ylidenes or imidazolin-2-ylidenes with dimethylcadmium. Four new carbene complexes are characterized by NMR spectroscopy (1H , 13C and 113Cd). The cadmium centers are strongly shifted downfield (100 -150 ppm) by interaction with the carbenes. X-ray structures are reported for three carbene-cadmium 1:1 adducts. The cadmium centers exhibit distorted trigonal-planar geometries in which the carbene ligands have an average 18.2 pm longer bond distance to cadmium compared to the methyl groups. The planes of cadmium coordination are twisted with respect to the plane of the imidazole ring. The more basic imidazolin-2-ylidene is shown to displace imidazol-2-ylidenes from the cadmium center.


2008 ◽  
Vol 14 (33) ◽  
pp. 10415-10422 ◽  
Author(s):  
Polly L. Arnold ◽  
Ian J. Casely ◽  
Zoë R. Turner ◽  
Christopher D. Carmichael

1983 ◽  
Vol 38 (11) ◽  
pp. 1313-1324 ◽  
Author(s):  
Klaus Ackermann ◽  
Peter Hofmann ◽  
Frank H. Köhler ◽  
Hans Kratzer ◽  
Herbert Krist ◽  
...  

Abstract A new one-step synthesis for bis-carbene complexes cis-M(CO)4L2 (M = Cr, Mo, W) containing cyclic carbene ligands L has been developed. These compounds can be oxidized by ferrocenium salts to paramagnetic cation complexes [M(CO)4L2]+ which, for M = Cr, are isolable in the form of their PF6 salts. The chromium compounds with L= 1,3-dimethyl-4-imidazolin-2-ylidene permit for the first time a structural and spectroscopic comparison of a diamagnetic carbene complex with the corresponding paramagnetic cation; the experimental facts are interpreted by molecular orbital calculations.


2020 ◽  
Vol 44 (14) ◽  
pp. 5343-5353
Author(s):  
Marco Baron ◽  
Anna Dall’Anese ◽  
Alessandro Miolato ◽  
Maddalena L. C. Cairoli ◽  
Valerio Di Marco ◽  
...  

Novel homoleptic gold(iii) complexes with bidentate N-heterocyclic carbene ligands have been successfully synthesised by transmetalation reaction and studied as anion sensors in solution by means of 1H NMR and UV-vis titration experiments.


2004 ◽  
Vol 43 (6) ◽  
pp. 2213-2219 ◽  
Author(s):  
Elena Mas-Marzá ◽  
Macarena Poyatos ◽  
Mercedes Sanaú ◽  
Eduardo Peris

2018 ◽  
Vol 54 (88) ◽  
pp. 12429-12438 ◽  
Author(s):  
Peter V. Simpson ◽  
Marco Falasca ◽  
Massimiliano Massi

Rhenium tricarbonyl complexes bound to N-heterocyclic carbene ligands are emerging as a new class of complexes with promising applications in a wide variety of areas.


2012 ◽  
Vol 23 (5) ◽  
pp. 486-497 ◽  
Author(s):  
Rosenani A. Haque ◽  
H. Zetty Zulikha ◽  
Mohammed Z. Ghdhayeb ◽  
Srinivasa Budagumpi ◽  
Abbas Washeel Salman

2019 ◽  
Vol 48 (2) ◽  
pp. 653-663 ◽  
Author(s):  
Linh M. Quan ◽  
Bradley D. Stringer ◽  
Mohammad A. Haghighatbin ◽  
Johnny Agugiaro ◽  
Gregory J. Barbante ◽  
...  

A series of electrochemiluminescent iridium(iii) N-heterocyclic carbene complexes have been prepared to tune electrochemical and spectroscopic behaviour.


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