High-energy metal to ligand charge-transfer states in ruthenium-diimine complexes

1989 ◽  
Vol 93 (20) ◽  
pp. 7099-7107 ◽  
Author(s):  
Michael L. Myrick ◽  
M. Keith De Armond
Keyword(s):  
Charge Transfer ◽  
High Energy ◽  
Ligand Charge Transfer ◽  
Diimine Complexes ◽  
Ruthenium Diimine Complexes

Long-lived MLCT states for Ru(ii) complexes of ferrocene-appended 2,2′-bipyridines

2019 ◽  
Vol 48 (41) ◽  
pp. 15713-15722 ◽  
Author(s):  
Jonathan E. Barnsley ◽  
James A. Findlay ◽  
Georgina E. Shillito ◽  
William S. Pelet ◽  
Synøve Ø. Scottwell ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Ligand Charge Transfer ◽  
Diimine Complexes

In this study, we present two ruthenium(ii) diimine complexes appended with ferrocene which show metal to ligand charge transfer 3MLCT emission lifetimes around 630 ns.

Photophysics of Re(I) and Ru(II) Diimine Complexes Covalently Linked to Pyrene: Contributions from Intra-Ligand Charge Transfer States

2002 ◽  
Vol 41 (2) ◽  
pp. 359-366 ◽  
Author(s):  
Del Guerzo ◽  
Stéphanie Leroy ◽  
Frédéric Fages ◽  
Russell H. Schmehl
Keyword(s):  
Charge Transfer ◽  
Ligand Charge Transfer ◽  
Covalently Linked ◽  
Diimine Complexes

scholarly journals Probing CuI in homogeneous catalysis using high-energy-resolution fluorescence-detected X-ray absorption spectroscopy

2015 ◽  
Vol 51 (48) ◽  
pp. 9864-9867 ◽  
Author(s):  
Richard C. Walroth ◽  
Jacob W. H. Uebler ◽  
Kyle M. Lancaster
Keyword(s):  
Charge Transfer ◽  
Homogeneous Catalysis ◽  
Energy Resolution ◽  
Catalytic Reaction ◽  
High Energy ◽  
High Energy Resolution ◽  
X Ray ◽  
Ligand Charge Transfer ◽  
X Ray Absorption ◽  
Absorption Features

CuI X-ray absorption features are assigned as metal-to-ligand charge transfer bands. These features facilitate species identification in catalytic reaction mixtures.

Synthesis and Photochemical Properties of Re(I) Tricarbonyl Complexes Bound to Thione and Thiazole-2-ylidene Ligands

2020 ◽  
Author(s):  
Matthew Stout ◽  
Brian Skelton ◽  
Alexandre N. Sobolev ◽  
Paolo Raiteri ◽  
Massimiliano Massi ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Excited States ◽  
Ligand Exchange ◽  
Ligand Substitution ◽  
Bidentate Ligand ◽  
The Other ◽  
Ligand Exchange Reaction ◽  
Multiple Products ◽  
Ligand Charge Transfer ◽  
Photochemical Properties

<p>Three Re(I) tricarbonyl complexes, with general formulation Re(N^L)(CO)<sub>3</sub>X (where N^L is a bidentate ligand containing a pyridine functionalized in the position 2 with a thione or a thiazol-2-ylidene group and X is either chloro or bromo) were synthesized and their reactivity explored in terms of solvent-dependent ligand substitution, both in the ground and excited states. When dissolved in acetonitrile, the complexes bound to the thione ligand underwent ligand exchange with the solvent resulting in the formation of Re(NCMe)<sub>2</sub>(CO)<sub>3</sub>X. The exchange was found to be reversible, and the starting complex was reformed upon removal of the solvent. On the other hand, the complexes appeared inert in dichloromethane or acetone. Conversely, the complex bound to the thiazole-2-ylidene ligand did not display any ligand exchange reaction in the dark, but underwent photoactivated ligand substitution when excited to its lowest metal-to-ligand charge transfer manifold. Photolysis of this complex in acetonitrile generated multiple products, including Re(I) tricarbonyl and dicarbonyl solvato-complexes as well as free thiazole-2-ylidene ligand.</p>

scholarly journals Tuning π-Acceptor/σ-Donor Ratio of the 2-Isocyanoazulene Ligand: Non-Fluorinated Rival of Pentafluorophenyl Isocyanide and Trifluorovinyl Isocyanide Discovered

Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 981
Author(s):  
Mason D. Hart ◽  
John J. Meyers ◽  
Zachary A. Wood ◽  
Toshinori Nakakita ◽  
Jason C. Applegate ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Coordination Chemistry ◽  
Single Crystal ◽  
13C Nmr ◽  
Quantitative Assessment ◽  
X Ray ◽  
New Class ◽  
Linear Relationships ◽  
Ligand Charge Transfer ◽  
Donor Characteristics

Isocyanoazulenes (CNAz) constitute a relatively new class of isocyanoarenes that offers rich structural and electronic diversification of the organic isocyanide ligand platform. This article considers a series of 2-isocyano-1,3-X2-azulene ligands (X = H, Me, CO2Et, Br, and CN) and the corresponding zero-valent complexes thereof, [(OC)5Cr(2-isocyano-1,3-X2-azulene)]. Air- and thermally stable, X-ray structurally characterized 2-isocyano-1,3-dimethylazulene may be viewed as a non-benzenoid aromatic congener of 2,6-dimethyphenyl isocyanide (2,6-xylyl isocyanide), a longtime “workhorse” aryl isocyanide ligand in coordination chemistry. Single crystal X-ray crystallographic {Cr–CNAz bond distances}, cyclic voltametric {E1/2(Cr0/1+)}, 13C NMR {δ(13CN), δ(13CO)}, UV-vis {dπ(Cr) → pπ*(CNAz) Metal-to-Ligand Charge Transfer}, and FTIR {νN≡C, νC≡O, kC≡O} analyses of the [(OC)5Cr(2-isocyano-1,3-X2-azulene)] complexes provided a multifaceted, quantitative assessment of the π-acceptor/σ-donor characteristics of the above five 2-isocyanoazulenes. In particular, the following inverse linear relationships were documented: δ(13COtrans) vs. δ(13CN), δ(13COcis) vs. δ(13CN), and δ(13COtrans) vs. kC≡O,trans force constant. Remarkably, the net electron withdrawing capability of the 2-isocyano-1,3-dicyanoazulene ligand rivals those of perfluorinated isocyanides CNC6F5 and CNC2F3.

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