4.7 Article

Rapid build up of nanooptomechanical transduction in single crystals of a ruthenium-based SO2 linkage photoisomer

期刊

CHEMICAL COMMUNICATIONS
卷 57, 期 11, 页码 1320-1323

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cc06755e

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资金

  1. Science and Technology Facilities Council via the ISIS Neutron and Muon Facility
  2. U.S. Department of Energy (DOE) Office of Science, Office of Basic Energy Sciences
  3. 1851 Royal Commission of the Great Exhibition
  4. U.S. DOE [DE-AC02-06CH11357]
  5. Division of Chemistry (CHE), National Science Foundation (NSF) [NSF/CHE-1346572, NSF/CHE-1834750]
  6. NSF [NSF/DMR-1531283]
  7. National Council of Science and Technology of Mexico (CONACyT) [217553]
  8. Cambridge Trust [217553]
  9. Division of Materials Research (DMR), National Science Foundation (NSF) [NSF/CHE-1346572, NSF/CHE-1834750]

向作者/读者索取更多资源

This study reveals the phenomenon of single-crystal nanooptomechanical transduction under specific conditions of light stimulation, along with the changes in molecular structure that occur during this process.
Single-crystal nanooptomechanical transduction occurs in [Ru(SO2)(NH3)(4)(H2O)]chlorobenzenesulfonate(2), reaching maximal levels within 40 s at 100 K when photostimulated by 505 nm light. Its in situ light-induced crystal structure reveals the molecular origins of this optical actuation: 26.0(3)% of the eta(1)-SO2 ligand photoconverts into an eta(1)-OSO photoisomer which, in turn, induces a 49.6(9)degrees arene ring rotation in its neighbouring counter ion.

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