Organometallic chemistry of carbaporphyrinoids: synthesis and characterization of nickel(ii) and palladium(ii) azuliporphyrinsPart 20 of the series ‘Conjugated Macrocycles Related to the Porphyrins’. Part 19: S. R. Graham, D. A. Colby and T. D. Lash, Angew. Chem., 2002, in press.

2002 ◽  
pp. 894-895 ◽  
Author(s):  
Shelley R. Graham ◽  
Gregory M. Ferrence ◽  
Timothy D. Lash
2020 ◽  
Vol 49 (11) ◽  
pp. 3473-3479 ◽  
Author(s):  
Volodymyr Levchenko ◽  
Cristiano Glessi ◽  
Sigurd Øien-Ødegaard ◽  
Mats Tilset

The synthesis and characterization of a series of N-heterocyclic Au(iii) carbene complexes prepared by oxidation of (NHC)AuCl in aqua regia is described.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Zhe Huang ◽  
Yongliang Zhang ◽  
Wen-Xiong Zhang ◽  
Junnian Wei ◽  
Shengfa Ye ◽  
...  

AbstractAs aromaticity is one of the most fundamental concepts in chemistry, the construction of aromatic systems has long been an important subject. Herein, we report the synthesis and characterization of a tris-spiroaromatic complex, hexalithio spiro vanadacycle 2. The delocalization of the four electrons within the two V 3d orbitals and the π* orbitals of the three biphenyl ligands leads to a 40π Craig-Möbius aromatic system with three metalla-aromatic rings, as revealed by both experimental measurements and theoretical analyses. For comparison, if Cr is used instead of V, a similar Craig-Möbius aromatic system can not be generated. In this case, pentalithio spiro chromacycle 3 is obtained, and the Cr center uses its two 3d orbitals to form two independent metalla-aromatic rings. This work presents a type of aromatic systems that will contribute to both aromaticity theory and organometallic chemistry.


Molecules ◽  
2021 ◽  
Vol 26 (22) ◽  
pp. 6838
Author(s):  
Christos Lampropoulos ◽  
Gabriel Rashad ◽  
Chris Douvris

The organometallic chemistry of metal complexes with organocyclic ligands of higher than five hapticity is much more lacking than the chemistry of metal complexes with η5-cyclopentadienyl ligands, which has been explored in considerable depth, resulting in novel advances. The main reason for this is stability. In particular, reports indicate that (η7-C7H7)MLn complexes are considerably less stable than analogous (η5-C5H5)MLn. In perfluoroalkyl metal chemistry, there is currently no reported (η7-C7H7)MLn derivative, whereas a number of alkylated ones are known and important conclusions have been drawn about their stability. Responding to this void, and using Morrison’s trifluoromethylating reagent, the present study reports the synthesis and characterization of the first cycloheptatrienyl molybdenum complexes bearing the trifluoromethyl moiety; (η7-C7H7)Mo(CO)2CF3 (I), and (η7-C7H7)Mo(CO)(PMe3)CF3 (II) and discusses their low thermal instability.


1992 ◽  
Vol 31 (5) ◽  
pp. 928-930 ◽  
Author(s):  
Francoise Quignard ◽  
Christine Lecuyer ◽  
Catherine Bougault ◽  
Frederic Lefebvre ◽  
Agnes Choplin ◽  
...  

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