TY - JOUR
T1 - Pyrene Appended Free-base, Phosphorus(V) and Gallium(III) Corroles and Their β,β′-Linked Corrole Dimers
T2 - Synthesis, Photophysical and Electrochemical Properties
AU - Sujesh, S.
AU - Basumatary, Biju
AU - Kumar, Amit
AU - Sankar, Jeyaraman
N1 - Funding Information:
S.S acknowledges DST-INSPIRE for junior research fellowship. B.B. acknowledges UGC for the SRF Fellowship. A.K acknowledges IISER Bhopal for research funding. The facilities and infrastructure provided by IISER Bhopal are highly acknowledged. JS acknowledges SERB, New Delhi for the grant EMR/2016/005768.
Funding Information:
S.S acknowledges DST‐INSPIRE for junior research fellowship. B.B. acknowledges UGC for the SRF Fellowship. A.K acknowledges IISER Bhopal for research funding. The facilities and infrastructure provided by IISER Bhopal are highly acknowledged. JS acknowledges SERB, New Delhi for the grant EMR/2016/005768.
Publisher Copyright:
© 2020 Wiley-VCH GmbH
PY - 2021/2/12
Y1 - 2021/2/12
N2 - Pyrene appended free-base, phosphorus(V) and gallium (III) corrole conjugates were synthesized and characterized. Efficient β-β′ dimerization of corroles was achieved by oxidation with p-chloranil in moderate yield from their respective metallated corroles. The weak ground state electronic coupling between pyrene and corrole units was established by photophysical and electrochemical investigations. The fluorescence spectral studies showed a red shifted emission maximum for dimer with respect to their monomeric counterpart due to possible π-conjugation and supported by the density functional theory (DFT). The electrochemical investigation revealed multiple oxidation associated with the corrole and pyrene centers.
AB - Pyrene appended free-base, phosphorus(V) and gallium (III) corrole conjugates were synthesized and characterized. Efficient β-β′ dimerization of corroles was achieved by oxidation with p-chloranil in moderate yield from their respective metallated corroles. The weak ground state electronic coupling between pyrene and corrole units was established by photophysical and electrochemical investigations. The fluorescence spectral studies showed a red shifted emission maximum for dimer with respect to their monomeric counterpart due to possible π-conjugation and supported by the density functional theory (DFT). The electrochemical investigation revealed multiple oxidation associated with the corrole and pyrene centers.
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U2 - 10.1002/ejic.202000807
DO - 10.1002/ejic.202000807
M3 - Article
AN - SCOPUS:85100165884
SN - 1434-1948
VL - 2021
SP - 540
EP - 547
JO - European Journal of Inorganic Chemistry
JF - European Journal of Inorganic Chemistry
IS - 6
ER -