On the Effect of a Single Solvent Molecule on the Charge-Transfer Band of a Donor–Acceptor Anion

2013 ◽  
Vol 135 (18) ◽  
pp. 6818-6821 ◽  
Author(s):  
Jørgen Houmøller ◽  
Marius Wanko ◽  
Kristian Støchkel ◽  
Angel Rubio ◽  
Steen Brøndsted Nielsen
Keyword(s):  
Charge Transfer ◽  
Charge Transfer Band ◽  
Solvent Molecule ◽  
Donor Acceptor

The Coulomb Shift of the Charge Transfer Band in Donor- Acceptor Compounds

1981 ◽  
Vol 108 (2) ◽  
pp. 399-404
Author(s):  
I. D. Mikhailov ◽  
S. V. Novikov ◽  
A. V. Vannieov
Keyword(s):  
Charge Transfer ◽  
Charge Transfer Band ◽  
Donor Acceptor

Ultrafast Charge Transfer and Relaxation at a Donor–Acceptor Interface

2021 ◽  
Author(s):  
Fernando Rodríguez Díaz ◽  
Hong-Guang Duan ◽  
R. J. Dwayne Miller ◽  
Michael Thorwart
Keyword(s):  
Charge Transfer ◽  
Donor Acceptor ◽  
Ultrafast Charge Transfer

Homoleptic 2,2′-bipyridine metalates(–I) of iron and cobalt, one cocrystallized with an anthracene radical anion and the other with neutral anthracene

2014 ◽  
Vol 70 (8) ◽  
pp. 828-832
Author(s):  
William W. Brennessel ◽  
John E. Ellis
Keyword(s):  
Radical Anion ◽  
Complex Cation ◽  
Solvent Molecule ◽  
Inversion Center ◽  
Asymmetric Unit ◽  
Aromatic Donor ◽  
Donor Acceptor ◽  
Anthracene Molecule ◽  
Packing Arrangement ◽  
Solvent Molecules

Homoleptic 2,2′-bipyridine (bipy) metalates of iron and cobalt have been synthesized directly from the corresponding homoleptic anthracene metalates. In the iron structure, bis[([2.2.2]cryptand)potassium(I)] tris(2,2′-bipyridine)ferrate(–I) anthracene(–I), [K(C18H36N2O6)]2[Fe(C10H8N2)3](C14H10), the asymmetric unit contains one potassium complex cation in a general position, the Fe center and one and a half bipy ligands of the ferrate complex on a crystallographic twofold axis that includes the Fe atom, and one half of an anthracene radical anion whose other half is generated by a crystallographic inversion center. The cations and anions are well separated and the geometry about the Fe center is essentially octahedral. In the cobalt structure, ([2.2.2]cryptand)potassium(I) bis(2,2′-bipyridine)cobaltate(–I) anthracene hemisolvate tetrahydrofuran (THF) disolvate, [K(C18H36N2O6)][Co(C10H8N2)2]·0.5C14H10·2C4H8O, the asymmetric unit contains the cation, anion, and both cocrystallized THF solvent molecules in general positions, and one half of a cocrystallized anthracene molecule whose other half is generated by a crystallographic inversion center. The cation and anion are well separated and the ligand planes in the cobaltate anion are periplanar. Each anthracene molecule is midway between and is oriented perpendicular to a pair of symmetry-related bipy ligands such that aromatic donor–acceptor interactions may play a role in the packing arrangement. The lengths of the bonds that connect the bipy rings support the assertion that the ligands are bipy radical anions in the iron structure. However, in the case of cobalt, these lengths are between the known ranges for a bipy radical anion and a bipy dianion, and therefore no conclusion can be made from the crystallography alone. One cocrystallized THF solvent molecule in the cobalt structure was modeled as disordered over three positions with appropriate geometric and thermal restraints, which resulted in a refined component mass ratio of 0.412 (4):0.387 (3):0.201 (3).

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