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Structural isolation of NIR absorbing ferrocenyl bridged N-confused fused expanded phlorin, N-confused porphodimethene and the π-extended corrorin isomer: synthesis and characterization.

Buddhadeb ChakrabortySumit SahooRaja NarayansamyDandamudi UsharaniHarapriya Rath
Published in: Dalton transactions (Cambridge, England : 2003) (2021)
Concise syntheses and spectroscopic, solid state X-ray crystal structure and theoretical studies of three electronically appealing new generation hitherto unknown ferrocenyl bridged N-confused heterocyclic macrocycles with (without) fusion are reported. Intriguingly, the expanded N-confused fused phlorin (1.1.1.1.1) with the built-in tripentacyclic [5.5.5] moiety exhibits tailing of the NIR absorption band beyond 1000 nm while the nonconjugated porphodimethene and a new generation π-extended isomeric corrorin analogue exhibit UV-vis absorption.
Keyphrases
  • crystal structure
  • solid state
  • photodynamic therapy
  • fluorescence imaging
  • high resolution
  • fluorescent probe
  • drug release
  • molecular docking
  • magnetic resonance imaging
  • magnetic resonance
  • mass spectrometry