TY - JOUR
T1 - Dipole moments of polyenic oligomeric systems. Part II - Molecular organic wire resistivities
T2 - Polyacetylenes, allenes and polyynes
AU - Morales, Raul G.E.
AU - González-Rojas, Claudio
PY - 2005/9
Y1 - 2005/9
N2 - Polyacetylenic, allenic and polyynic molecular wire series, containing electron-donor (D) and electron-acceptor (A) groups as two terminal units of the oligomeric bridge (D-wire-A), can be well described by means of a one-dimensional conduction model, which considers a scattering process of electrons through the charge-transfer conduction bridge. The conduction constants (γi) of the oligomeric structures of the three molecular series under study were determined from the functional dependence between the dipole moment of the oligomers (μn) and the π-molecular orbital bridge length (L). According to our one-dimensional molecular organic wire model: μn = μo + μ∞ (1 - e-γL) where μo is the dipolar moment of the first compound of the oligomeric series without a bridge unit (n = 0) and μ∞ is a limit value for L → ∞. By means of the Landauer theoretical expression for the conductance of a metallic one-dimensional conductor and our molecular wire conduction constants (γi), we determined the intrinsic resistivities associated with the molecular resistances of these oligomeric wires. Using this approach we determined, for the first time, the linear and non-linear contributions to the net molecular resistivity. The order of magnitudes of the linear resistivities determined in these oligomeric systems agrees very well with the expected results of experimental measurements for macroscopic wires.
AB - Polyacetylenic, allenic and polyynic molecular wire series, containing electron-donor (D) and electron-acceptor (A) groups as two terminal units of the oligomeric bridge (D-wire-A), can be well described by means of a one-dimensional conduction model, which considers a scattering process of electrons through the charge-transfer conduction bridge. The conduction constants (γi) of the oligomeric structures of the three molecular series under study were determined from the functional dependence between the dipole moment of the oligomers (μn) and the π-molecular orbital bridge length (L). According to our one-dimensional molecular organic wire model: μn = μo + μ∞ (1 - e-γL) where μo is the dipolar moment of the first compound of the oligomeric series without a bridge unit (n = 0) and μ∞ is a limit value for L → ∞. By means of the Landauer theoretical expression for the conductance of a metallic one-dimensional conductor and our molecular wire conduction constants (γi), we determined the intrinsic resistivities associated with the molecular resistances of these oligomeric wires. Using this approach we determined, for the first time, the linear and non-linear contributions to the net molecular resistivity. The order of magnitudes of the linear resistivities determined in these oligomeric systems agrees very well with the expected results of experimental measurements for macroscopic wires.
KW - Conduction constants
KW - Dipole moments
KW - Molecular resisitivities
KW - Oligomers
UR - https://www.scopus.com/pages/publications/23244434895
U2 - 10.1002/poc.931
DO - 10.1002/poc.931
M3 - Article
AN - SCOPUS:23244434895
SN - 0894-3230
VL - 18
SP - 941
EP - 944
JO - Journal of Physical Organic Chemistry
JF - Journal of Physical Organic Chemistry
IS - 9
ER -