Time-resolved spectroscopic study on chiral supramolecules consist of bis(zinc octaethylporphyrin) and (R)- and (S)-diaminocyclohexanes using; transient absorption, CD,and EPR spectroscopies.
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| Title: | Time-resolved spectroscopic study on chiral supramolecules consist of bis(zinc octaethylporphyrin) and (R)- and (S)-diaminocyclohexanes using; transient absorption, CD,and EPR spectroscopies. |
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| Authors: | Murakami, Makoto1 (AUTHOR), Imai, Ken1 (AUTHOR), Ida, Takahito1 (AUTHOR), Araki, Yasuyuki1 (AUTHOR) y.araki@tohoku.ac.jp, Wada, Takehiko1 (AUTHOR), Yamauchi, Seigo1 (AUTHOR), Kobori, Yasuhiro2 (AUTHOR), Ito, Osamu1 (AUTHOR) |
| Source: | Research on Chemical Intermediates. Mar2026, Vol. 52 Issue 3, p1949-1963. 15p. |
| Subjects: | Time-resolved spectroscopy, Circular dichroism, Triplet state (Quantum mechanics), Absorption spectra, Organic compounds, Electron paramagnetic resonance spectroscopy, Supramolecules, Porphyrins |
| Abstract: | We developed a new method to measure the time-resolved CD (TR-CD) spectra of the photo-excited triplet states of chiral supramolecules of bis(zinc octaethylporphyrin) and (R)- and (S)-diaminocyclohexane in the wide wavelength region (UV and visible) even overlapping with the intense steady-state CD signals. Such measurements are possible by developing a high-sensitive TR-CD equipment assembled in our laboratory. The observed TR-CD spectra of the triplet states of chiral supramolecules show mono-signate CD signals corresponding to each transient absorption band in the 300–500-nm region. Combination of the TR-CD spectral pattern with the dynamic behavior of the CD signals in the excited triplet states affords information for the electron distribution change of the triplet state from that of the ground state. In addition, the zero-field splitting parameters obtained from the time-resolved EPR spectra of the photo-excited supramolecules suggest that the electron spin density distributes on one side of two porphyrin rings of the chiral bis-porphyrin supramolecules in the triplet states, which is further confirmed by the DFT calculations. [ABSTRACT FROM AUTHOR] |
| Copyright of Research on Chemical Intermediates is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: egs DbLabel: Engineering Source An: 192009809 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Time-resolved spectroscopic study on chiral supramolecules consist of bis(zinc octaethylporphyrin) and (R)- and (S)-diaminocyclohexanes using; transient absorption, CD,and EPR spectroscopies. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Murakami%2C+Makoto%22">Murakami, Makoto</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Imai%2C+Ken%22">Imai, Ken</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ida%2C+Takahito%22">Ida, Takahito</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Araki%2C+Yasuyuki%22">Araki, Yasuyuki</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> y.araki@tohoku.ac.jp</i><br /><searchLink fieldCode="AR" term="%22Wada%2C+Takehiko%22">Wada, Takehiko</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yamauchi%2C+Seigo%22">Yamauchi, Seigo</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kobori%2C+Yasuhiro%22">Kobori, Yasuhiro</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ito%2C+Osamu%22">Ito, Osamu</searchLink><relatesTo>1</relatesTo> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Research+on+Chemical+Intermediates%22">Research on Chemical Intermediates</searchLink>. Mar2026, Vol. 52 Issue 3, p1949-1963. 15p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Time-resolved+spectroscopy%22">Time-resolved spectroscopy</searchLink><br /><searchLink fieldCode="DE" term="%22Circular+dichroism%22">Circular dichroism</searchLink><br /><searchLink fieldCode="DE" term="%22Triplet+state+%28Quantum+mechanics%29%22">Triplet state (Quantum mechanics)</searchLink><br /><searchLink fieldCode="DE" term="%22Absorption+spectra%22">Absorption spectra</searchLink><br /><searchLink fieldCode="DE" term="%22Organic+compounds%22">Organic compounds</searchLink><br /><searchLink fieldCode="DE" term="%22Electron+paramagnetic+resonance+spectroscopy%22">Electron paramagnetic resonance spectroscopy</searchLink><br /><searchLink fieldCode="DE" term="%22Supramolecules%22">Supramolecules</searchLink><br /><searchLink fieldCode="DE" term="%22Porphyrins%22">Porphyrins</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: We developed a new method to measure the time-resolved CD (TR-CD) spectra of the photo-excited triplet states of chiral supramolecules of bis(zinc octaethylporphyrin) and (R)- and (S)-diaminocyclohexane in the wide wavelength region (UV and visible) even overlapping with the intense steady-state CD signals. Such measurements are possible by developing a high-sensitive TR-CD equipment assembled in our laboratory. The observed TR-CD spectra of the triplet states of chiral supramolecules show mono-signate CD signals corresponding to each transient absorption band in the 300–500-nm region. Combination of the TR-CD spectral pattern with the dynamic behavior of the CD signals in the excited triplet states affords information for the electron distribution change of the triplet state from that of the ground state. In addition, the zero-field splitting parameters obtained from the time-resolved EPR spectra of the photo-excited supramolecules suggest that the electron spin density distributes on one side of two porphyrin rings of the chiral bis-porphyrin supramolecules in the triplet states, which is further confirmed by the DFT calculations. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Research on Chemical Intermediates is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s11164-025-05893-x Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 15 StartPage: 1949 Subjects: – SubjectFull: Time-resolved spectroscopy Type: general – SubjectFull: Circular dichroism Type: general – SubjectFull: Triplet state (Quantum mechanics) Type: general – SubjectFull: Absorption spectra Type: general – SubjectFull: Organic compounds Type: general – SubjectFull: Electron paramagnetic resonance spectroscopy Type: general – SubjectFull: Supramolecules Type: general – SubjectFull: Porphyrins Type: general Titles: – TitleFull: Time-resolved spectroscopic study on chiral supramolecules consist of bis(zinc octaethylporphyrin) and (R)- and (S)-diaminocyclohexanes using; transient absorption, CD,and EPR spectroscopies. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Murakami, Makoto – PersonEntity: Name: NameFull: Imai, Ken – PersonEntity: Name: NameFull: Ida, Takahito – PersonEntity: Name: NameFull: Araki, Yasuyuki – PersonEntity: Name: NameFull: Wada, Takehiko – PersonEntity: Name: NameFull: Yamauchi, Seigo – PersonEntity: Name: NameFull: Kobori, Yasuhiro – PersonEntity: Name: NameFull: Ito, Osamu IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: Mar2026 Type: published Y: 2026 Identifiers: – Type: issn-print Value: 09226168 Numbering: – Type: volume Value: 52 – Type: issue Value: 3 Titles: – TitleFull: Research on Chemical Intermediates Type: main |
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