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Articles

Self-assembly of zinc chlorophyll derivatives possessing a pyrenyl group at the 17-propionate residue and effects of additional γ-cyclodextrins on their optical properties

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Pages 753-760 | Received 30 Sep 2013, Accepted 06 Nov 2013, Published online: 07 Jan 2014
 

Abstract

Two kinds of zinc 31-hydroxy-131-oxo-chlorins 1 and 2 possessing a pyrenyl group at the 17-propionate residue, of which the linker length between the chlorin and the pyrene moieties was varied, were synthesised from naturally occurring chlorophyll a, and were self-assembled in an aqueous solution. Both zinc chlorins 1 and 2 exhibited Qy absorption bands around 720 nm accompanying circular dichroism signals in the Qy region, indicating that these zinc chlorins could form self-aggregates like chlorosomes of green photosynthetic bacteria. Addition of γ-cyclodextrin into an aqueous solution containing the self-aggregates of zinc chlorin 1 esterified with 1-pyrenylmethanol induced the appearance of excimer emission of the pyrene moieties around 480 nm as well as increased the fluorescence intensities of the pyrene monomers at 378 and 396 nm, while only an increase in fluorescence from the monomeric pyrene moiety was observed in the case of 2 esterified with 4-(1-pyrenyl)butanol. Exogenous γ-cyclodextrin unchanged the spectral features derived from the chlorin moieties of 1 and 2 in the aqueous phase. These suggest that the encapsulation of the pyrenyl groups in the zinc chlorins unchanged their assembling states under the present conditions.

Acknowledgements

The authors thank Prof. Tomohiro Miyatake, Ryukoku University for HRMS measurements.

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