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- Publisher Website: 10.1002/chem.201405035
- Scopus: eid_2-s2.0-84925168302
- PMID: 25693972
- WOS: WOS:000352504500024
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Article: Supramolecular Assembly of Achiral Alkynylplatinum(II) Complexes and Carboxylic β‐1,3‐Glucan into Different Helical Handedness Stabilized by Pt⋅⋅⋅Pt and/or π–π Interactions
Title | Supramolecular Assembly of Achiral Alkynylplatinum(II) Complexes and Carboxylic β‐1,3‐Glucan into Different Helical Handedness Stabilized by Pt⋅⋅⋅Pt and/or π–π Interactions |
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Authors | |
Keywords | Chirality Circular dichroism Helical structures Platinum Supramolecular chemistry |
Issue Date | 2015 |
Publisher | Wiley - V C H Verlag GmbH & Co. KGaA. |
Citation | Chemistry: A European Journal, 2015, v. 21 n. 14, p. 5447-5458 How to Cite? |
Abstract | Two‐component ensembles of alkynylplatinum(II) terpyridine (tpy) complexes and carboxylic β‐1,3‐glucan (CurCOOH) have been investigated by using spectroscopic and microscopic techniques, as well as time‐dependent UV/Vis absorption and circular dichroism (CD) experiments. Microscopic images of [Pt(tpy){CCC6H4(CH2NMe3‐4)}](OTf)2 (1) have revealed spherical nanostructures, whereas helical fibrous structures of different lengths, depending on the concentration of complex 1 and CurCOOH, were observed. The helical assemblies have been found to show low‐energy metal‐metal‐to‐ligand charge transfer (MMLCT) absorption and triplet MMLCT (3MMLCT) emission, which are indicative of Pt⋅⋅⋅Pt and/or π–π interactions between the complex 1 molecules. Interestingly, the ensemble has been demonstrated to show different handedness and even a change in handedness over time under different experimental conditions. Low temperatures, low concentrations of CurCOOH, high concentrations of complex 1, or successive addition of CurCOOH into complex 1 solution favor the formation of right‐handed helical assemblies, whereas high temperatures, high concentrations of CurCOOH, low concentrations of complex 1, or single‐batch addition of CurCOOH into complex 1 solution result in a fast chiroptical inversion of the ensemble solution, giving rise to the left‐handed helical assemblies as the dominant species. The results have been rationalized by considering the competing kinetically and thermodynamically controlled assembly–elongation of the ensemble, which leads to the formation of right‐handed and left‐handed helical assemblies, respectively. The change in the handedness of the ensemble has been demonstrated to stem from the formation of two‐component assemblies with supramolecular interactions, in contrast to the template‐ induced chiral amplification commonly observed in other systems. |
Persistent Identifier | http://hdl.handle.net/10722/215096 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.058 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Chung, CYS | - |
dc.contributor.author | Tamaru, SI | - |
dc.contributor.author | Shinkai, S | - |
dc.contributor.author | Yam, VWW | - |
dc.date.accessioned | 2015-08-21T12:27:11Z | - |
dc.date.available | 2015-08-21T12:27:11Z | - |
dc.date.issued | 2015 | - |
dc.identifier.citation | Chemistry: A European Journal, 2015, v. 21 n. 14, p. 5447-5458 | - |
dc.identifier.issn | 0947-6539 | - |
dc.identifier.uri | http://hdl.handle.net/10722/215096 | - |
dc.description.abstract | Two‐component ensembles of alkynylplatinum(II) terpyridine (tpy) complexes and carboxylic β‐1,3‐glucan (CurCOOH) have been investigated by using spectroscopic and microscopic techniques, as well as time‐dependent UV/Vis absorption and circular dichroism (CD) experiments. Microscopic images of [Pt(tpy){CCC6H4(CH2NMe3‐4)}](OTf)2 (1) have revealed spherical nanostructures, whereas helical fibrous structures of different lengths, depending on the concentration of complex 1 and CurCOOH, were observed. The helical assemblies have been found to show low‐energy metal‐metal‐to‐ligand charge transfer (MMLCT) absorption and triplet MMLCT (3MMLCT) emission, which are indicative of Pt⋅⋅⋅Pt and/or π–π interactions between the complex 1 molecules. Interestingly, the ensemble has been demonstrated to show different handedness and even a change in handedness over time under different experimental conditions. Low temperatures, low concentrations of CurCOOH, high concentrations of complex 1, or successive addition of CurCOOH into complex 1 solution favor the formation of right‐handed helical assemblies, whereas high temperatures, high concentrations of CurCOOH, low concentrations of complex 1, or single‐batch addition of CurCOOH into complex 1 solution result in a fast chiroptical inversion of the ensemble solution, giving rise to the left‐handed helical assemblies as the dominant species. The results have been rationalized by considering the competing kinetically and thermodynamically controlled assembly–elongation of the ensemble, which leads to the formation of right‐handed and left‐handed helical assemblies, respectively. The change in the handedness of the ensemble has been demonstrated to stem from the formation of two‐component assemblies with supramolecular interactions, in contrast to the template‐ induced chiral amplification commonly observed in other systems. | - |
dc.language | eng | - |
dc.publisher | Wiley - V C H Verlag GmbH & Co. KGaA. | - |
dc.relation.ispartof | Chemistry: A European Journal | - |
dc.subject | Chirality | - |
dc.subject | Circular dichroism | - |
dc.subject | Helical structures | - |
dc.subject | Platinum | - |
dc.subject | Supramolecular chemistry | - |
dc.title | Supramolecular Assembly of Achiral Alkynylplatinum(II) Complexes and Carboxylic β‐1,3‐Glucan into Different Helical Handedness Stabilized by Pt⋅⋅⋅Pt and/or π–π Interactions | - |
dc.type | Article | - |
dc.identifier.email | Chung, CYS: cyschung@hku.hk | - |
dc.identifier.email | Yam, VWW: wwyam@hku.hk | - |
dc.identifier.authority | Chung, CYS=rp02672 | - |
dc.identifier.authority | Yam, VWW=rp00822 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/chem.201405035 | - |
dc.identifier.pmid | 25693972 | - |
dc.identifier.scopus | eid_2-s2.0-84925168302 | - |
dc.identifier.hkuros | 246383 | - |
dc.identifier.volume | 21 | - |
dc.identifier.issue | 14 | - |
dc.identifier.spage | 5447 | - |
dc.identifier.epage | 5458 | - |
dc.identifier.isi | WOS:000352504500024 | - |
dc.publisher.place | Germany | - |
dc.identifier.issnl | 0947-6539 | - |