meso ‐Pyrrole‐Substituted 22‐Oxacorroles: Building Blocks for the Synthesis of BODIPY‐Bridged 22‐Oxacorrole Dyads | Zendy

Kalita Hemanta | Zendy; Ravikanth Mangalampalli | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

meso ‐Pyrrole‐Substituted 22‐Oxacorroles: Building Blocks for the Synthesis of BODIPY‐Bridged 22‐Oxacorrole Dyads

Author(s) -

Kalita Hemanta,

Ravikanth Mangalampalli

Publication year - 2015

Publication title -

chemistry – a european journal

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.687

H-Index - 242

eISSN - 1521-3765

pISSN - 0947-6539

DOI - 10.1002/chem.201500702

Subject(s) - bodipy , synthon , pyrrole , chemistry , boron , yield (engineering) , electrochemistry , reactivity (psychology) , combinatorial chemistry , nanotechnology , stereochemistry , materials science , organic chemistry , fluorescence , physics , electrode , medicine , alternative medicine , quantum mechanics , pathology , metallurgy

Novel boron‐dipyrromethene (BODIPY)‐bridged 22‐oxacorrole dyads, using meso ‐pyrrolyl 22‐oxacorrole as a key synthon, have been synthesized. The reactivity of the meso ‐pyrrolyl group of 22‐oxacorrole was exploited to synthesize the first examples of BODIPY‐bridged 22‐oxacorrole dyads in ≈40 % yield. The dyads are stable and exhibited interesting spectral and electrochemical properties.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research