Optical Activity of Transition Metal Compounds. I. Sector Rules for Metal Complexes of the Pseudotetragonal Class

1971 ◽  
Vol 54 (6) ◽  
pp. 2453-2468 ◽  
Author(s):  
F. S. Richardson
1993 ◽  
Vol 48 (2) ◽  
pp. 189-194 ◽  
Author(s):  
Christoph Schmidt ◽  
Wolfgang Beck ◽  
Christoph Schmidt ◽  
Wolfgang Beck

AbstractThe dianions of epindolidione and dimethylepindolidione act as bis(chelate) ligands (L) and form deep red polymeric complexes [L′ML]n (M = Ni(II), Co(II); L′ = DMF, PEt3). They react with chloro bridged complexes [(R3P)MCl2]2 (M = Pd, Pt) and [(η5-C5Me5)MCl2]2 (M = Rh, Ir) to give red bis-N,O-chelate complexes (R3P)(Cl)M-μ-L-M (Cl)(PR3) and (η5-C5H5)(Cl)M -μ-L-M(Cl)(η5-C5H5).


2020 ◽  
Vol 44 (6) ◽  
pp. 2281-2290
Author(s):  
Wei Xi ◽  
Fu-Qiang Song ◽  
Xue-Li Xia ◽  
Xue-Qin Song

The structure and DNA binding performance of three transition metal compounds based on a new pyrazolone ligand were tuned effectively by changing both metal cations and anions.


1972 ◽  
Vol 27 (11) ◽  
pp. 1332-1335 ◽  
Author(s):  
Hans G. Biedermann ◽  
Josef Obwandner ◽  
Klaus Wichmann

Atactic poly-4-vinylpyridine forms with transition metal compounds in ethyl alcohol the following complexes: Me (II) L2 (P-4-VP-m)2 and Me (II) J2 (P-4-VP-m)3, Me = Fe, Co, Ni. L = Cl⁻, acetylacetonate, salicylaldehydate and o-nitrophenolate. The IR-spectra are discussed.


Author(s):  
R. Morris Bullock ◽  
Geoffrey M. Chambers

This perspective examines frustrated Lewis pairs (FLPs) in the context of heterolytic cleavage of H 2 by transition metal complexes, with an emphasis on molecular complexes bearing an intramolecular Lewis base. FLPs have traditionally been associated with main group compounds, yet many reactions of transition metal complexes support a broader classification of FLPs that includes certain types of transition metal complexes with reactivity resembling main group-based FLPs. This article surveys transition metal complexes that heterolytically cleave H 2 , which vary in the degree that the Lewis pairs within these systems interact. Many of the examples include complexes bearing a pendant amine functioning as the base with the metal functioning as the hydride acceptor. Consideration of transition metal compounds in the context of FLPs can inspire new innovations and improvements in transition metal catalysis. This article is part of the themed issue ‘Frustrated Lewis pair chemistry’.


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