Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1626
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dc.contributor.authorWackerlin, Christianen_US
dc.contributor.authorSiewert, Dorotaen_US
dc.contributor.authorJung, Thomas A.en_US
dc.contributor.authorBALLAV, NIRMALYAen_US
dc.date.accessioned2019-02-14T05:01:22Z
dc.date.available2019-02-14T05:01:22Z
dc.date.issued2013-09en_US
dc.identifier.citationPhysical Chemistry Chemical Physics, 15(39), 16510-16514.en_US
dc.identifier.issn1463-9076en_US
dc.identifier.issn1463-9084en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1626-
dc.identifier.urihttps://doi.org/10.1039/C3CP50966Den_US
dc.description.abstractThe on-surface ligation of nitric oxide (NO) with Co-tetraphenylporphyrin (CoTPP) sublimed onto oxygen-reconstructed Ni(001) is studied using room-temperature scanning tunneling microscopy (STM) and complementary photoemission spectroscopies. On the oxygen-reconstructed substrates, the porphyrins are observed to form well-ordered, self-assembled layers. STM directly images the NO ligand as a characteristic feature in the center of the molecule. Under certain STM imaging conditions the dynamicity of this feature can be related to the temperature-activated conformational flexibility of the NO ligand. This provides an indirect confirmation of the bending of the Co–NO bond, as predicted from classical coordination chemistry.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectConformational freedomen_US
dc.subjectAxial liganden_US
dc.subjectCo-tetraphenylporphyrinen_US
dc.subjectSTM imaging conditionsen_US
dc.subjectClassical coordination chemistryen_US
dc.subject2013en_US
dc.titleOn-surface coordination chemistry: direct imaging of the conformational freedom of an axial ligand at room temperatureen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitlePhysical Chemistry Chemical Physicsen_US
dc.publication.originofpublisherForeignen_US
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