An anomalous behavior of the fluorescence of substituted oligothiophenes (α-α′ linkages) as a function of the number of rings has been reported. In this work we have theoretically investigated this phenomenon. Theoretical characterizations of both ground and excited states of oligothiophenes were carried out through the use of sophisticated semi-empirical methods. Our results have shown that the experimentally observed charge transfer suppression can be explained in terms of the evolution and the nature of the electronic configurations.8501/03/1511171118Roncali, J., (1992) Chem. Rev., 92, p. 711Dos Santos, D.A., Galvão, D.S., Laks, B., Dos Santos, M.C., (1991) Chem. Phys. Lett., 184, p. 579. , and references thereinKanemitsu, Y., Suzuki, K....
Excitation energies of neutral thiophene oligomers with chain lengths of up to 25 rings and charged ...
The photophysical properties of a series of 3,4-ethylenedioxythiophene oligomers (OEDOT) with up to ...
We investigate -conjugated oligomers with donor and acceptor groups using the DFT method and compare...
A comprehensive photophysical and spectroscopic (electronic and Raman) study guided by density funct...
We have analyzed singlet and triplet excitation energies in oligothiophenes (up to five rings) using...
A study of the structure, electronic, and optical properties of oligothiophenes is reported. Geometr...
The absorption and fluorescence properties of oligothiophenes in various solvents are reported at va...
The ground and excited-state properties of oligothiophenes connected by Si-atoms have been studied t...
In the present work we report on quantum chemical calculations of oligothiophenes. The conformation ...
The absorption and fluorescence properties of oligothiophenes in various solvents are reported at va...
We have studied optical properties of one-dimensional oligothiophenes and thiophene-based oligomers....
We present a comprehensive study of the optical and electronic properties of a series of oligothioph...
The phosphorescence spectra of a series of small oligothiophenes (nT, n = 1-3) incorporating a varie...
The electronic structure and stability of oligothiophene pairs (both neutral and positively charged)...
A large basis set of R-oligothiophenes with two to seven rings (R2-R7), also including thiophene, R1...
Excitation energies of neutral thiophene oligomers with chain lengths of up to 25 rings and charged ...
The photophysical properties of a series of 3,4-ethylenedioxythiophene oligomers (OEDOT) with up to ...
We investigate -conjugated oligomers with donor and acceptor groups using the DFT method and compare...
A comprehensive photophysical and spectroscopic (electronic and Raman) study guided by density funct...
We have analyzed singlet and triplet excitation energies in oligothiophenes (up to five rings) using...
A study of the structure, electronic, and optical properties of oligothiophenes is reported. Geometr...
The absorption and fluorescence properties of oligothiophenes in various solvents are reported at va...
The ground and excited-state properties of oligothiophenes connected by Si-atoms have been studied t...
In the present work we report on quantum chemical calculations of oligothiophenes. The conformation ...
The absorption and fluorescence properties of oligothiophenes in various solvents are reported at va...
We have studied optical properties of one-dimensional oligothiophenes and thiophene-based oligomers....
We present a comprehensive study of the optical and electronic properties of a series of oligothioph...
The phosphorescence spectra of a series of small oligothiophenes (nT, n = 1-3) incorporating a varie...
The electronic structure and stability of oligothiophene pairs (both neutral and positively charged)...
A large basis set of R-oligothiophenes with two to seven rings (R2-R7), also including thiophene, R1...
Excitation energies of neutral thiophene oligomers with chain lengths of up to 25 rings and charged ...
The photophysical properties of a series of 3,4-ethylenedioxythiophene oligomers (OEDOT) with up to ...
We investigate -conjugated oligomers with donor and acceptor groups using the DFT method and compare...