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dc.contributor.authorVummaleti, Sai V. C.
dc.contributor.authorNelson, David J.
dc.contributor.authorPoater, Albert
dc.contributor.authorGómez-Suárez, Adrián
dc.contributor.authorCordes, David B.
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorNolan, Steven P.
dc.contributor.authorCavallo, Luigi
dc.date.accessioned2017-06-06T08:02:37Z
dc.date.available2017-06-06T08:02:37Z
dc.date.issued2015
dc.identifier.citationVummaleti, S. V. C., Nelson, D. J., Poater, A., Gómez-Suárez, A., Cordes, D. B., Slawin, A. M. Z., … Cavallo, L. (2015). CCDC 1024811: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/cc13ddfb
dc.identifier.doi10.5517/cc13ddfb
dc.identifier.urihttp://hdl.handle.net/10754/624364
dc.description.abstractAn entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
dc.formatCIF
dc.language.isoeng
dc.publisherCambridge Crystallographic Data Centre
dc.subjectCrystal Structure
dc.subjectExperimental 3D Coordinates
dc.subjectCrystal System
dc.subjectSpace Group
dc.subjectCell Parameters
dc.subjectCrystallography
dc.subject1,3-Dimesityl-1,3-dihydro-2H-imidazole-2-selenone
dc.titleCCDC 1024811: Experimental Crystal Structure Determination : 1,3-Dimesityl-1,3-dihydro-2H-imidazole-2-selenone
dc.typeDataset
dc.contributor.departmentChemical Science Program
dc.contributor.departmentKAUST Catalysis Center (KCC)
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
kaust.personVummaleti, Sai V. C.
kaust.personCavallo, Luigi
dc.relation.issupplementtoDOI:10.1039/C4SC03264K
dc.identifier.ccdc1024811
display.relations<b> Is Supplement To:</b> <br/> <ul><li><i>[Article]</i> <br/> What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes? 2015, 6 (3):1895 Chem. Sci.. DOI: <a href="https://doi.org/10.1039/C4SC03264K">10.1039/C4SC03264K</a> HANDLE: <a href="http://hdl.handle.net/10754/550524">10754/550524</a></li></ul>


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