Jump to main content
Jump to site search

Issue 15, 2010
Previous Article Next Article

Extending conjugation in porphyrin dimer carbocations

Author affiliations

Abstract

The addition of alkynyl porphyrins to carbonyl compounds was used to prepare a series of porphyrin dimer tertiary alcohols. Treatment of these alcohols with acid gave conjugated carbocations with three to nine carbon atoms bridging between the porphyrins. All these carbocations show strong absorption in the near-IR region between 1000–1800 nm. The absorption spectra exhibit a length-dependence similar to that of polymethine cyanines, with a bathochromic shift of approximately 200 nm (900 cm−1) per alkyne. The longest of these chromophores has an absorption maximum at 1623 nm (in CHCl3 with 2% trifluoroacetic acid). The symmetry of the π-system has a strong effect on the position, intensity and width of the absorption bands. The stability of the cations in solution decreases with increasing bridge length.

Graphical abstract: Extending conjugation in porphyrin dimer carbocations

Back to tab navigation

Supplementary files

Publication details

The article was received on 04 Mar 2010, accepted on 21 May 2010 and first published on 04 Jun 2010


Article type: Paper
DOI: 10.1039/C003715J
Citation: Org. Biomol. Chem., 2010,8, 3472-3479
  •   Request permissions

    Extending conjugation in porphyrin dimer carbocations

    K. J. Thorley and H. L. Anderson, Org. Biomol. Chem., 2010, 8, 3472
    DOI: 10.1039/C003715J

Search articles by author

Spotlight

Advertisements