In the comproportionation reaction of Cu X and Cu with isopropylacetylene (iPr-C≡C-H), the ethynediide species C is generated via concomitant C-H/C-C bond cleavage of the iPr-C≡C-H precursor under moderate temperature to direct the formation of Cu mixed ethynediide/isopropylethynide nanoclusters (potentially explosive). The active ethynediide dianion C exhibits chameleon-like templating behavior to form C @Cu (m=6 (3, 4), 7 (2, 4), 8 (1)) central structural units for successive formation of {C ⊂Cu } (1, 2), {6 C ⊂Cu } (3), and {18 C ⊂Cu } (4) complexes. Bearing the highest C content, complex 4 features an unprecedented nanoscale Cu C kernel. Furthermore, 1-3 exhibit structure-controlled photoluminescence in the solid state.
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http://dx.doi.org/10.1002/anie.201708760 | DOI Listing |
Angew Chem Int Ed Engl
December 2017
Department of Chemistry and Center of Novel Functional Molecules, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR, P. R. China.
In the comproportionation reaction of Cu X and Cu with isopropylacetylene (iPr-C≡C-H), the ethynediide species C is generated via concomitant C-H/C-C bond cleavage of the iPr-C≡C-H precursor under moderate temperature to direct the formation of Cu mixed ethynediide/isopropylethynide nanoclusters (potentially explosive). The active ethynediide dianion C exhibits chameleon-like templating behavior to form C @Cu (m=6 (3, 4), 7 (2, 4), 8 (1)) central structural units for successive formation of {C ⊂Cu } (1, 2), {6 C ⊂Cu } (3), and {18 C ⊂Cu } (4) complexes. Bearing the highest C content, complex 4 features an unprecedented nanoscale Cu C kernel.
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