| Literature DB >> 25284044 |
Karl Börjesson1, Dušan Ćoso, Victor Gray, Jeffrey C Grossman, Jingqi Guan, Charles B Harris, Norbert Hertkorn, Zongrui Hou, Yosuke Kanai, Donghwa Lee, Justin P Lomont, Arun Majumdar, Steven K Meier, Kasper Moth-Poulsen, Randy L Myrabo, Son C Nguyen, Rachel A Segalman, Varadharajan Srinivasan, Willam B Tolman, Nikolai Vinokurov, K Peter C Vollhardt, Timothy W Weidman.
Abstract
A study of the scope and limitations of varying the ligand framework around the dinuclear core of FvRu2 in its function as a molecular solar thermal energy storage framework is presented. It includes DFT calculations probing the effect of substituents, other metals, and CO exchange for other ligands on ΔHstorage . Experimentally, the system is shown to be robust in as much as it tolerates a number of variations, except for the identity of the metal and certain substitution patterns. Failures include 1,1',3,3'-tetra-tert-butyl (4), 1,2,2',3'-tetraphenyl (9), diiron (28), diosmium (24), mixed iron-ruthenium (27), dimolybdenum (29), and ditungsten (30) derivatives. An extensive screen of potential catalysts for the thermal reversal identified AgNO3 -SiO2 as a good candidate, although catalyst decomposition remains a challenge.Entities:
Keywords: ab initio calculations; iron; isomerization; photochemistry; ruthenium
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Year: 2014 PMID: 25284044 DOI: 10.1002/chem.201404170
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236