Synthesis and properties of open-cage fullerene C60 derivatives: impact of the extended π-conjugation

2018 ◽  
Vol 2 (2) ◽  
pp. 206-213 ◽  
Author(s):  
Yoshifumi Hashikawa ◽  
Hidefumi Yasui ◽  
Kei Kurotobi ◽  
Yasujiro Murata

Novel open-cage fullerene C60 derivatives with extended π-conjugation bearing thiophene rings exhibit long wavelength absorption due to characteristic intramolecular charge transfer transitions.

1983 ◽  
Vol 48 (8) ◽  
pp. 2376-2385 ◽  
Author(s):  
Libuše Pavlíčková ◽  
Bohumír Koutek ◽  
Václav Jehlička ◽  
Milan Souček

Electronic spectra of 7,7-disubstituted quinone methides I-III with substituents of various electronegativities were measured in thirteen solvents. Character of the long-wavelength transition was investigated by correlation between transition energy and ionization potential of the donor part of the molecule as well as by comparison of transition moment with Δμ. The long wavelength absorption band of Ia-Id, IIa and IV does not correspond to a pure (π-π*) transition, but it is perturbed by intramolecular charge transfer.


1975 ◽  
Vol 6 (33) ◽  
pp. no-no
Author(s):  
ANTON J. DE GEE ◽  
WALTHERUS J. SEP ◽  
JAN W. VERHOEVEN ◽  
THYMEN J. DE BOER

2003 ◽  
Vol 58 (9) ◽  
pp. 922-924 ◽  
Author(s):  
Horst Kunkely ◽  
Arnd Vogler

The intense long-wavelength absorption of Naphthol Green B at λmax = 712 nm is assigned to a ligand-to-metal charge transfer (MLCT) transition. LMCT excitation of the complex in aqueous solution leads to the reduction of Fe(III) to Fe(II) with a quantum yield of ϕ = 1.14×10−3 at λirr = 577 nm.


1969 ◽  
Vol 23 (3) ◽  
pp. 254-256 ◽  
Author(s):  
A. Mustafa ◽  
R. Abu-Eittah ◽  
S. Elgendi

The electronic absorption spectra of some drugs derived from p-amino benzoic acid were studied. The effect of the substituent on the position of band maxima and intensity has been rationalized. Long wavelength energies have been found to agree well with calculated energies of the intramolecular charge transfer bands.


1998 ◽  
Vol 53 (2) ◽  
pp. 224-226 ◽  
Author(s):  
Horst Kunkely ◽  
Arnd Vogler

Abstract The electronic spectrum of Cp2TiS5 shows a long-wavelength absorption at λ max = 492 nm which is assigned to the lowest-energy S52- → TiIV ligand-to-metal charge transfer (LMCT) transition. The photolysis of the complex in CH2CI2 leads to the formation of Cp2TiCl2 and elemental sulfur. It is suggested that LMCT excitation initiates a reductive elimination with the extrusion of S5 while the reduced titanocene is reoxidized by the solvent.


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