Synthesis, crystal structure, and nonlinear optical behavior of beta-unsubstituted meso-meso E-vinylene-linked porphyrin dimers.
[structure: see text] A vinylene-linked porphyrin dimer, with no substituents at the beta-positions, has been synthesized by CuI/CsF promoted Stille coupling. In the crystal structure of this dimer, the C(2)H(2) bridge is twisted by 45 degrees relative to the plane of the porphyrins. The absorption,...
Main Authors: | Frampton, M, Akdas, H, Cowley, A, Rogers, J, Slagle, J, Fleitz, P, Drobizhev, M, Rebane, A, Anderson, H |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2005
|
Similar Items
-
MESO-ALKYNYL PORPHYRINS
by: Anderson, H
Published: (1992) -
The nonlinear optical characterization of meso-substituted porphyrin dyes
by: McEwan, K, et al.
Published: (2000) -
Reverse saturable absorption in the near-infrared by fused porphyrin dimers
by: McEwan, K, et al.
Published: (2004) -
Template-directed synthesis of strained meso-meso-linked porphyrin nanorings
by: Van Raden, JM, et al.
Published: (2024) -
Selective synthesis of β-unsubstituted meso-aryl substituted tripyrranes in water
by: Cheng-Zhi Gu, et al.
Published: (2015-03-01)