Literature DB >> 19053800

Phenylethynyl-BODIPY oligomers: bright dyes and fluorescent building blocks.

Yusuf Cakmak1, Engin U Akkaya.   

Abstract

Boradiazaindacene dyes were converted into phenylethynyl-BODIPY oligomers via a cycle of reactions, notably including Sonogashira couplings. As expected, as the number, n, of repeating units increases, peak absorption and emission wavelengths are shifted to the red end of the visible spectrum, albeit with smaller increments as n increases. Decyl groups help to keep the solubility remarkably high, and in addition to being very bright red-emitting fluorophores, their rigid rod-like structures could allow their use as functional building blocks.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19053800     DOI: 10.1021/ol802446e

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

Review 1.  Squaraine Dyes: Molecular Design for Different Applications and Remaining Challenges.

Authors:  Kristina Ilina; William M MacCuaig; Matthew Laramie; Jannatun N Jeouty; Lacey R McNally; Maged Henary
Journal:  Bioconjug Chem       Date:  2019-08-12       Impact factor: 4.774

2.  Brilliant BODIPY-fluorene Copolymers With Dispersed Absorption and Emission Maxima.

Authors:  Cliferson Thivierge; Aurore Loudet; Kevin Burgess
Journal:  Macromolecules       Date:  2011-05-24       Impact factor: 5.985

3.  Highly Efficient Solid-State Near-infrared Organic Light-Emitting Diodes incorporating A-D-A Dyes based on α,β-unsubstituted "BODIPY" Moieties.

Authors:  Andrea Zampetti; Alessandro Minotto; Benedetta Maria Squeo; Vasilis G Gregoriou; Sybille Allard; Ullrich Scherf; Christos L Chochos; Franco Cacialli
Journal:  Sci Rep       Date:  2017-05-09       Impact factor: 4.379

4.  Vinylene-Bridged Cyclic Dipyrrin and BODIPY Trimers.

Authors:  Songlin Xue; Daiki Kuzuhara; Naoki Aratani; Hiroko Yamada
Journal:  Int J Mol Sci       Date:  2020-10-28       Impact factor: 5.923

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.