Blackening of aza-BODIPY analogues by simple dimerization: Panchromatic absorption of a pyrrolopyrrole aza-BODIPY dimer

Yuto Kage, Shigeki Mori, Marina Ide, Akinori Saeki, Hiroyuki Furuta, Soji Shimizu

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Dimerization of the so-called pyrrolopyrrole aza-BODIPY, which is a new class of aza-BODIPY analogues exhibiting intense absorption and emission in the visible (Vis) and near infrared (NIR) region, via a bithienyl linkage led to the creation of a novel black dye with dual emission and panchromatic absorption properties in the Vis/NIR region. The role of the linkage in the dye was unambiguously elucidated by comparison of the optical properties with those of its biphenyl-linked counterpart.

Original languageEnglish
Pages (from-to)112-120
Number of pages9
JournalMaterials Chemistry Frontiers
Volume2
Issue number1
DOIs
Publication statusPublished - Jan 1 2018

Fingerprint

Dimerization
Dimers
Coloring Agents
Dyes
Infrared radiation
Optical properties
4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
diphenyl

All Science Journal Classification (ASJC) codes

  • Materials Chemistry
  • Materials Science(all)

Cite this

Blackening of aza-BODIPY analogues by simple dimerization : Panchromatic absorption of a pyrrolopyrrole aza-BODIPY dimer. / Kage, Yuto; Mori, Shigeki; Ide, Marina; Saeki, Akinori; Furuta, Hiroyuki; Shimizu, Soji.

In: Materials Chemistry Frontiers, Vol. 2, No. 1, 01.01.2018, p. 112-120.

Research output: Contribution to journalArticle

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