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      Synthesis, spectroscopic and crystallographic analysis of the Zn-complex of a di( β, β′-sulfoleno)pyrrin: model for Zn-complexes of bilirubin and of phylloxanthobilins

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          Abstract

          Abstract

          A high yield preparation, spectroscopic and crystallographic investigation of the crystalline Zn-complex of a di( β, β′-sulfoleno)pyrrin are reported here. In the brightly green fluorescent Zn-complex of the hardly luminescent di( β, β′-sulfoleno)pyrrin, the metal ion is bound by two di( β, β′-sulfoleno)pyrrin ligands, as revealed first by its mass spectra. The crystal structure of this Zn-complex of the di( β, β′-sulfoleno)pyrrin confirmed a regular 2:1 composition of the bidentate di( β, β′-sulfoleno)pyrrin ligand and the metal ion. The latter was coordinated in a distorted tetrahedral fashion, as found in other dipyrrin Zn-complexes. The here studied Zn-complex of a designed di( β, β′-sulfoleno)pyrrin ligand provides insights into the coordination properties of the proposed (2:1)- and (2:2)-complexes of phylloxanthobilin and bilirubin, respectively, which are two abundant natural bilin-type tetrapyrroles.

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          A photofunctional bottom-up bis(dipyrrinato)zinc(II) complex nanosheet

          Two-dimensional polymeric nanosheets have recently gained much attention, particularly top-down nanosheets such as graphene and metal chalcogenides originating from bulk-layered mother materials. Although molecule-based bottom-up nanosheets manufactured directly from molecular components can exhibit greater structural diversity than top-down nanosheets, the bottom-up nanosheets reported thus far lack useful functionalities. Here we show the design and synthesis of a bottom-up nanosheet featuring a photoactive bis(dipyrrinato)zinc(II) complex motif. A liquid/liquid interfacial synthesis between a three-way dipyrrin ligand and zinc(II) ions results in a multi-layer nanosheet, whereas an air/liquid interfacial reaction produces a single-layer or few-layer nanosheet with domain sizes of >10 μm on one side. The bis(dipyrrinato)zinc(II) metal complex nanosheet is easy to deposit on various substrates using the Langmuir–Schäfer process. The nanosheet deposited on a transparent SnO2 electrode functions as a photoanode in a photoelectric conversion system, and is thus the first photofunctional bottom-up nanosheet.
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            Selective manipulation of ICT and PET Processes in styryl-Bodipy derivatives: applications in molecular logic and fluorescence sensing of metal ions.

            Remarkably versatile chemistry of Bodipy dyes allows the design and straightforward synthesis of multivalent-multitopic derivatives, which, with judicious selection of metal ion-ligand pairs based on known affinities, affords control and manipulation of photoinduced electron transfer and internal charge transfer processes as desired. We have demonstrated that metal ions acting as modulators (or inputs, in digital design parlance) can generate absorbance changes in accordance with the operation of a half-adder. In addition, an AND logic gate in the emission mode was delivered using a different binucleating arrangement of ligands. A molecular equivalent of a three-input AND logic gate was also obtained exploiting differential binding affinities of metal ions for different ligands. The results suggest that different metal ions can be used as nonannihilating inputs, selectively targeting various ligands incorporated within a single fluorophore, and with careful design, diverse photophysical processes can be selectively modulated, resulting in a range of signals, useful in molecular logic design, and offering an enticing potential for multianalyte chemosensors.
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              Bright, color-tunable fluorescent dyes in the visible-near-infrared region.

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                Author and article information

                Contributors
                bernhard.kraeutler@uibk.ac.at
                Journal
                Monatsh Chem
                Monatsh. Chem
                Monatshefte Fur Chemie
                Springer Vienna (Vienna )
                0026-9247
                1434-4475
                21 April 2016
                21 April 2016
                2016
                : 147
                : 1031-1036
                Affiliations
                [ ]Institute of Organic Chemistry and Centre of Molecular Biosciences, University of Innsbruck, 6020 Innsbruck, Austria
                [ ]School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300072 People’s Republic of China
                [ ]Institute of General, Inorganic and Theoretical Chemistry, University of Innsbruck, 6020 Innsbruck, Austria
                Article
                1748
                10.1007/s00706-016-1748-0
                4863038
                27226652
                7aedb3e5-8e73-4094-a1e9-1b4075138286
                © The Author(s) 2016

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 27 February 2016
                : 21 March 2016
                Funding
                Funded by: Austrian Academic Cooperation and Mobility Unit
                Award ID: WTZ CN 14/2007
                Award Recipient :
                Funded by: Tianjin International Cooperation Program of Science and Technology
                Award ID: 08ZCGHHZ00400
                Award Recipient :
                Funded by: Austrian National Science Foundation
                Award ID: I-563
                Award ID: P-28522
                Award Recipient :
                Categories
                Original Paper
                Custom metadata
                © Springer-Verlag Wien 2016

                crystal structure,dipyrrin,fluorescence spectroscopy,coordination chemistry,zn-complex

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