Cooperative Self-Assembly of Double-Strand Conjugated Porphyrin Ladders
摘要:
A series of conjugated zinc porphyrin oligomers, from the dimer through to the hexamer, form stable ladder complexes with linear bidentate ligands such as 1,4-diazabicyclo[2.2.2]octane (DABCO) and 4,4'-bipyridyl (Bipy). The H-1 NMR spectra of these ladders confirm their structures and show how they fray and dissociate in the presence of excess ligand. The thermodynamics of these equilibria were elucidated by spectrophotometric titration, using multivariate global factor analysis, in two different solvents (chloroform and toluene). Ladder formation and dissociation exhibit many indications of positive cooperativity, including all-or-nothing two-state assembly, sigmoidal isotherms, large Hill coefficients, and narcissistic self-sorting. Ladder formation increases the planarity and conjugation, resulting in a reduction in the gap between the highest occupied and lowest unoccupied molecular orbitals.
DOI:
10.1021/ja992821d
作为产物:
描述:
、 1,4-二碘苯 在
tris(dibenzylideneacetone)dipalladium (0) Me2NSnMe3 、 PPh3 作用下,
以
not given 为溶剂,
以61%的产率得到
参考文献:
名称:
Enhanced Electronic Conjugation in Anthracene-Linked Porphyrins
摘要:
Despite their larger separation, the porphyrin groups in 1 are more strongly conjugated than in analogous compounds in which butadiyne is the bridging unit. This stronger electronic coupling in 1 results in a bathochromic shift in its absorption and emission spectra.