Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2753
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dc.contributor.authorVenkataramani, Sugumar-
dc.date.accessioned2020-12-07T09:07:34Z-
dc.date.available2020-12-07T09:07:34Z-
dc.date.issued2014-
dc.identifier.citationDalton Transactions, 43(46), pp.17395-17405.en_US
dc.identifier.otherhttps://doi.org/10.1039/C4DT03048F-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2014/dt/c4dt03048f#!divAbstract-
dc.identifier.urihttp://hdl.handle.net/123456789/2753-
dc.descriptionAuthors sequences are not necessary in order-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractExtensive use of quantum chemical calculations has been made to rationally design a molecule whose spin state can be switched reversibly using light of two different wavelengths at room temperature in solution. Spin change is induced by changing the coordination number of a nickel complex. The coordination number in turn is switched using a photochromic ligand that binds in one configuration and dissociates in the other. We demonstrate that successful design relies on a precise geometry fit and delicate electronic tuning. Our designer complex exhibits an extremely high long-term switching stability (more than 20 000 cycles) and a high switching efficiency. The high-spin state is extraordinarily stable with a half-life of 400 days at room temperature. Switching between the dia- and paramagnetic state is achieved with visible light (500 and 430 nm). The compound can also be used as a molecular logic gate with light and pH as input and the magnetic state as non-destructive read-out.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectPhotochromic Liganden_US
dc.subjectParamagnetic Stateen_US
dc.subjectNickel Complexen_US
dc.titleRational design of a room temperature molecular spin switch. The light-driven coordination induced spin state switch (LD-CISSS) approachen_US
dc.typeArticleen_US
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