TY - JOUR
T1 - Periphery-fused chiral A2B-type subporphyrin
AU - Hirokawa, Shoma
AU - Kobayashi, Nagao
AU - Shimizu, Soji
N1 - Funding Information:
Funding: This work was supported by Grants-in-Aid for Scientific Research (B), Scientific Research (C) and Scientific Research on Innovative Areas, “pi-system Figuration: Control of Electron and Structural Dynamism for Innovative Functions (no. 2601)” (JSPS KAKENHI Grant numbers JP19H02703, JP18K05076, JP15H01001, and JP17H05160).
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/2/2
Y1 - 2021/2/2
N2 - Despite significant interest, the chiroptical properties of subporphyrins have rarely been investigated because chiral subporphyrins are elusive. Here, inherently chiral subporphyrins are elaborated by forming a fused pyran ring at the periphery of an A2B-type meso-aryl-substituted subporphyrin. Their circular dichroism (CD) properties are largely affected by the peripheral substituents and the dihedral angles between the meso-aryl substituents and the subporphyrin core: The β-perbromo subporphyrin with an orthogonal arrangement of the meso-phenyl substituents to the subporphyrin core exhibits weak CD signals corresponding to the Q bands, whereas the unsubstituted species with smaller dihedral angles shows relatively intense CD signals. A detailed structure-property relationship of these chiral subporphyrins was elucidated by time-dependent (TD) DFT calculations. This study reveals that the CD properties of chiral subporphyrins can be controlled by peripheral substitution and meso-aryl substituents.
AB - Despite significant interest, the chiroptical properties of subporphyrins have rarely been investigated because chiral subporphyrins are elusive. Here, inherently chiral subporphyrins are elaborated by forming a fused pyran ring at the periphery of an A2B-type meso-aryl-substituted subporphyrin. Their circular dichroism (CD) properties are largely affected by the peripheral substituents and the dihedral angles between the meso-aryl substituents and the subporphyrin core: The β-perbromo subporphyrin with an orthogonal arrangement of the meso-phenyl substituents to the subporphyrin core exhibits weak CD signals corresponding to the Q bands, whereas the unsubstituted species with smaller dihedral angles shows relatively intense CD signals. A detailed structure-property relationship of these chiral subporphyrins was elucidated by time-dependent (TD) DFT calculations. This study reveals that the CD properties of chiral subporphyrins can be controlled by peripheral substitution and meso-aryl substituents.
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U2 - 10.3390/molecules26041140
DO - 10.3390/molecules26041140
M3 - Article
C2 - 33672731
AN - SCOPUS:85102680841
SN - 1420-3049
VL - 26
JO - Molecules
JF - Molecules
IS - 4
M1 - 1140
ER -