Engineering Cofacial Trizinc(II)porphyrin Trimers: Linking Molecular Architecture with Excited-State Dynamics

We report a rational design of donor–acceptor–donor (D–A–D) Zn(II)porphyrin trimers adopting two conformational architectures, ABA (“ closed ”) and ACA (“ open ”), in which electron-rich terminal porphyrins flank an electron-deficient central unit linked by a flexible spacer. Minor variations in peripheral substitution at the central porphyrin trigger substantial structural reorganization, leading to pronounced differences in electronic coupling and excited-state behavior. The “ closed ” ABA architecture enforces close interchromophoric proximity, resulting in strong excitonic coupling and perturbation of the Soret band. In contrast, the “ open ” ACA conformer exhibits weaker coupling and minimal spectral distortion. As a result, ACA displays fluorescence resembling a linear superposition of its constituent monomers and a relatively long excited-state lifetime (∼3 ns). By comparison, ABA deviates significantly from monomeric behavior, consistent with enhanced intramolecular charge-transfer (ICT) interactions that shorten the fluorescence lifetime (∼800 ps) and suppress the fluorescence quantum yield. The more efficient ICT in ABA facilitates triplet-state formation, resulting in substantially higher singlet oxygen quantum yield than ACA . Accordingly, ABA exhibits superior photocatalytic activity, achieving quantitative oxidation of triphenylphosphine, whereas ACA shows markedly lower efficiency. Collectively, these results demonstrate that conformational modulation of excitonic and charge-transfer interactions provides an effective strategy for selective photooxidation.

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Publication Details

Journal
Inorganic Chemistry
Published
2026-06-29
DOI
https://doi.org/10.1021/acs.inorgchem.6c01566
Primary Topic
Porphyrin and Phthalocyanine Chemistry
Type
article
Field-Weighted Citation Impact
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article

Engineering Cofacial Trizinc(II)porphyrin Trimers: Linking Molecular Architecture with Excited-State Dynamics

Chandrani Pal, Dolly Chandel, Sankar Prasad Rath, Juwon Oh et al.
Inorganic Chemistry
Porphyrin and Phthalocyanine Chemistry
article

Engineering Cofacial Trizinc(II)porphyrin Trimers: Linking Molecular Architecture with Excited-State Dynamics

Chandrani Pal, Dolly Chandel, Sankar Prasad Rath, Juwon Oh, Jiwon Kim, Jaehyeok Ryu, Jiyeon Lee
article en

Abstract

We report a rational design of donor–acceptor–donor (D–A–D) Zn(II)porphyrin trimers adopting two conformational architectures, ABA (“ closed ”) and ACA (“ open ”), in which electron-rich terminal porphyrins flank an electron-deficient central unit linked by a flexible spacer. Minor variations in peripheral substitution at the central porphyrin trigger substantial structural reorganization, leading to pronounced differences in electronic coupling and excited-state behavior. The “ closed ” ABA architecture enforces close interchromophoric proximity, resulting in strong excitonic coupling and perturbation of the Soret band. In contrast, the “ open ” ACA conformer exhibits weaker coupling and minimal spectral distortion. As a result, ACA displays fluorescence resembling a linear superposition of its constituent monomers and a relatively long excited-state lifetime (∼3 ns). By comparison, ABA deviates significantly from monomeric behavior, consistent with enhanced intramolecular charge-transfer (ICT) interactions that shorten the fluorescence lifetime (∼800 ps) and suppress the fluorescence quantum yield. The more efficient ICT in ABA facilitates triplet-state formation, resulting in substantially higher singlet oxygen quantum yield than ACA . Accordingly, ABA exhibits superior photocatalytic activity, achieving quantitative oxidation of triphenylphosphine, whereas ACA shows markedly lower efficiency. Collectively, these results demonstrate that conformational modulation of excitonic and charge-transfer interactions provides an effective strategy for selective photooxidation.

Inorganic Chemistry
Yonsei University (KR), Kyungpook National University (KR), Hodges University (US), Integrative Medicine Institute (US), Green Chemistry (PL), Indian Institute of Technology Kanpur (IN)
Indian Institute of Technology Kanpur, National Research Foundation of Korea, Science and Engineering Research Board
Sustainable cities and communities
Openalex Percentile: Top 16%
Porphyrin and Phthalocyanine Chemistry
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