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The complex [((i)Pr(3)PCu)(2)(Me(2)Ga)(2)(SCH(2)CH(2)S)(2)] (4) was synthesized from trimethylgallium, [((i)Pr(3)PCu)(4)(SCH(2)CH(2)S)(2)] (1) and ethanedithiol by elimination of methane. The related monomethyl compound [((i)Pr(3)PCu)(2)(MeGaSPh)(2)(SCH(2)CH(2)S)(2)] (5) has been prepared from [((i)Pr(3)PCuSPh)(3)] (2) and [(MeGaSCH(2)CH(2)S)(2)] (3) by a ligand exchange reaction in tetrahydrofuran solution. The molecular structures of 1 and 3-5 were determined by single crystal X-ray diffraction. Thermolysis of 4 and 5 results in the formation of the ternary semiconductor CuGaS(2), gallite. The residue of 5 was characterized using X-ray powder diffraction, energy dispersive X-ray spectroscopy and transmission electron microscopy. The CuGaS(2) crystals obtained are mainly hexagonal plates of around 200 to 300 nm diameter and 10 to 30 nm thickness, exhibiting an unusual metastable hexagonal crystal structure, related to wurtzite. Partially, the usual tetragonal chalcopyrite structure or its disordered cubic zinc-blende analogue is realized by stacking faults, resulting in an overall similarity to the zinc-blende-wurtzite polytypism in ZnS and related compounds.
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http://dx.doi.org/10.1039/c2dt30904a | DOI Listing |
Bismuth oxychloride (BiOCl) is well known for its photocatalytic activity and many methods are reported to prepare this layered-structure material. In this study, bismuth hexafluoroacetylacetonate Bi(C5HF6O2)3 was chosen as Bi source in the synthesis of BiOCl. Uniform BiOCl nanoplates were fabricated without any organic additive to control the morphology.
View Article and Find Full Text PDFSci Rep
August 2017
BIOSCOPE Group, UCIBIO@REQUIMTE, Chemistry Department, Faculty of Science and Technology, University NOVA of Lisbon, Caparica, 2829-516, Portugal.
Dalton Trans
August 2015
Institute of Inorganic Chemistry and Center for Nanointegration Duisburg-Essen (CeNIDE), University of Duisburg-Essen, Universitätsstr. 5-7, D-45117 Essen, Germany.
Thermolysis of the single source precursor (Et2Bi)2Te in DIPB at 80 °C yielded phase-pure Bi4Te3 nanoparticles, while mixtures of Bi4Te3 and elemental Bi were formed at higher temperatures. In contrast, cubic Bi2Te particles were obtained by thermal decomposition of Et2BiTeEt in DIPB. Moreover, a dual source approach (hot injection method) using the reaction of Te(SiEt3)2 and Bi(NMe2)3 was applied for the synthesis of different pure Bi-Te phases including Bi2Te, Bi4Te3 and Bi2Te3, which were characterized by PXRD, REM, TEM and EDX.
View Article and Find Full Text PDFNanoscale
May 2014
Institut für Anorganische Chemie und Strukturchemie, Heinrich-Heine-Universität Düsseldorf, 40204 Düsseldorf, Germany.
Efforts to replace noble-metal catalysts by low-cost alternatives are of constant interest. The organometallic, non-aqueous wet-chemical synthesis of various hitherto unknown nanocrystalline Ni/Ga intermetallic materials and the use of NiGa for the selective semihydrogenation of alkynes to alkenes are reported. Thermal co-hydrogenolysis of the all-hydrocarbon precursors [Ni(COD)2] (COD = 1,5-cyclooctadiene) and GaCp* (Cp* = pentamethylcyclopentadienyl) in high-boiling organic solvents mesitylene and n-decane in molar ratios of 1 : 1, 2 : 3 and 3 : 1 yields the nano-crystalline powder materials of the over-all compositions NiGa, Ni2Ga3 and Ni3Ga, respectively.
View Article and Find Full Text PDFACS Appl Mater Interfaces
November 2013
Department of Chemistry and NASA-URC Center for Advanced Nanoscale Materials, University of Puerto Rico, San Juan 00936-8377, Puerto Rico.
A single-source approach was used to synthesize bimetallic nanoparticles on a high-surface-area carbon-support surface. The synthesis of palladium and palladium-cobalt nanoparticles on carbon black (Vulcan XC-72R) by chemical and thermal reduction using organometallic complexes as precursors is described. The electrocatalysts studied were Pd/C, Pd2Co/C, and PdCo2/C.
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