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Inorganic-Organic Hybrid Materials: Layered Zinc Hydroxide Salts with Intercalated Porphyrin Sensitizers
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SYSNO ASEP 0349658 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Inorganic-Organic Hybrid Materials: Layered Zinc Hydroxide Salts with Intercalated Porphyrin Sensitizers Author(s) Demel, Jan (UACH-T) SAI, RID, ORCID
Kubát, Pavel (UFCH-W) RID, ORCID, SAI
Jirka, Ivan (UFCH-W) RID, ORCID
Kovář, P. (CZ)
Pospíšil, M. (CZ)
Lang, Kamil (UACH-T) SAI, RID, ORCIDSource Title Journal of Physical Chemistry C. - : American Chemical Society - ISSN 1932-7447
Roč. 114, č. 39 (2010), s. 16321-16328Number of pages 8 s. Language eng - English Country US - United States Keywords molecular-dynamics simulations ; photophysical properties ; meso-tetratolylporphyrins Subject RIV CA - Inorganic Chemistry R&D Projects GAP207/10/1447 GA ČR - Czech Science Foundation (CSF) CEZ AV0Z40320502 - UACH-T (2005-2011) AV0Z40400503 - UFCH-W (2005-2011) UT WOS 000282209800034 DOI 10.1021/jp106116n Annotation Layered materials provide a two-dimensional interlayer space suitable for accommodating molecules with a designed functionality. In this study, inorganic-organic hybrids were prepared by intercalation of anionic porphyrin sensitizers into the host structure of layered zinc hydroxide salts. The inorganic host offers stabilization and protection, whereas the guest species provide the photofunction. The properties and arrangement of porphyrin molecules in the interlayer space were studied by a combination of experimental techniques and molecular simulations. Intercalation of porphyrins led to a gallery height that is comparable with the size of porphyrin molecules. Molecular simulations showed that the interlayer space is filled with disordered porphyrin units. The porphyrin sulfonate groups interact with the brucite-like layers via dominant electrostatic interactions similarly to layered double hydroxides. Workplace Institute of Inorganic Chemistry Contact Jana Kroneislová, krone@iic.cas.cz, Tel.: 311 236 931 Year of Publishing 2011
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