Synthesis and crystal structure of a cumulenic quinoidal porphyrin dimer with strong electronic absorption in the infrared
Quinoidalization results in amazingly intense near-IR absorption in 1 (λ(max) = 1080 nm), whereas the shorter dimer 2 (λ(max) = 780 nm) is less conjugated because steric interactions force it into a contorted geometry. The crystal structure of 1 shows that the 62-atom chromophore is bow-shaped in th...
Main Authors: | Blake, I, Rees, L, Claridge, T, Anderson, H |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2000
|
Similar Items
-
Synthesis and Crystal Structure of a Cumulenic Quinoidal Porphyrin Dimer with Strong Electronic Absorption in the Infrared We thank the Engineering and Physical Sciences Research Council (UK) and the Defence Evaluation and Research Agency (DERA, UK) for support and the EPSRC Mass Spectrometry Service in Swansea for FAB mass spectra.
by: Blake, I, et al.
Published: (2000) -
Fusion and planarization of a quinoidal porphyrin dimer.
by: Blake, I, et al.
Published: (2002) -
Push–pull quinoidal porphyrins
by: Smith, M, et al.
Published: (2018) -
Conjugated quinoidal porphyrin oligomers.
by: Anderson, H, et al.
Published: (2001) -
Porphyrin dimer carbocations with strong near infrared absorption and third-order optical nonlinearity.
by: Thorley, K, et al.
Published: (2008)