Tuning the photochemical properties of the fulvalene-tetracarbonyl-diruthenium system-Reference-Cited by-同舟云学术

Tuning the photochemical properties of the fulvalene-tetracarbonyl-diruthenium system

Published:2016 Issue:21 Volume:45 Page:8740-8744
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Lennartson Anders¹²³⁴,Lundin Angelica¹²³⁴,Börjesson Karl¹²³⁴⁵^ORCID,Gray Victor¹²³⁴,Moth-Poulsen Kasper¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry and Chemical Engineering

2. Chalmers University of Technology

3. SE-412 96 Gothenburg

4. Sweden

5. Present address: Department of Chemistry and Molecular Biology

Abstract

In a Molecular Solar–Thermal Energy Storage (MOST) system, solar energy is converted to chemical energy using a compound that undergoes reversible endothermic photoisomerization.

Funder

Vetenskapsrådet

Knut och Alice Wallenbergs Stiftelse

Swedish Foundation for Strategic Research

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/DT/C6DT01343K

Reference43 articles.

1. F. Weigert , Jahrbuch für Photographie, Kinematographie und Reproduktionsverfahren, 1909, p. 109

2. Chem. Abstr., 1910, 4, 3170

3. Bridged Polycyclic Compounds. VI. The Photoisomerization of Bicyclo [2,2,1]hepta-2,5-diene-2,3-dicarboxylic Acid to Quadricyclo [2,2,1,02,6,03,5]heptane-2,3-dicarboxylic Acid1,2

4. Photochemical transformations—VIII

5. PHOTOSENSITIZED CYCLOADDITION REACTIONS1

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