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Relevant academic research and scientific papers

CuI/iodine-mediated homocoupling reaction of terminal alkynes to 1,3-diynes

A facile and efficient pathway for CuI/iodine-mediated homocoupling reaction of terminal alkynes to symmetrical 1,4-disubstituted 1,3-diynes in good to excellent yields was reported.

Synthesis and photophysical properties of platinum(II) arylacetylides with donor-acceptor structures

The detailed relationship between the structure and the nonlinear mechanisms, as well as whether different nonlinear mechanisms of an organic molecule restrain each other are still not clear. In this paper, eight platinum(II) arylacetylides with donor-acceptor structures were synthesized and their photophysical properties were studied systematically. The properties of HOMO and LUMO were calculated using DFT method, the contribution of the metal dπ and charge transfer process are dominated by the skeleton structure of these complexes. The ligand-to-metal charge transfer (LMCT) happens when the molecule with D-π-Pt-π-D or D-π-Pt-π-Ar-π-Pt-π-D skeleton is excited, however the metal-to-ligand charge transfer (MLCT) and ligand-to-ligand charge transfer (LLCT) happen when the molecule with D-π-Pt-π-A, A-π-Pt-π-A or A-π-Pt-π-Ar-π-Pt-π-A skeleton is excited, respectively. The weak absorption in the visible area of these molecules provides a wide observation window for the application in optical limiter. The low fluorescent quantum yields and detectable room temperature phosphorescence indicate that the system-cross quantum yields of the title complexes containing Pt(II) is effective because of the spin-orbit coupling between the d orbitals of the Pt(II) and the large π-conjugated system. The first-order polarizabilities |βXXX| was determined by the solvatochromic method between 1.02 × 10-29 to 3.46 × 10-28 (cm5/esu).

Synthesis of 1,3-Diynes Using Calcium Carbide as an Alkyne Source

A simple method for the synthesis of 1,3-diynes from iodoarenes using calcium carbide as an alkyne source and air as an oxidant is described. A series of 1,4-diarylbuta-1,3-diynes were efficiently synthesized by this strategy. The salient features of this protocol are the use of inexpensive and easy-to-handle alkyne source, broad substrate scope, open-air condition, and simple operation procedure.

High-efficiency catalyst for copper nanoparticles attached to porous nitrogen-doped carbon materials: Applied to the coupling reaction of alkyne groups under mild conditions

Supported catalysts have attracted extensive attention due to their excellent catalytic performance and reliability in heterogeneous catalysis. In this work, we report a general synthesis strategy that achieves the self-coupling reaction of acetylene deri

Copper Nanoparticles on Ordered Mesoporous Carbon Nitride Support: a Superior Catalyst for Homo- and Cross-Coupling of Terminal Alkynes under Base-Free Conditions

A novel ordered mesoporous carbon nitride (OMCN) was synthesized as a functionalized support with 2,4,6-trichloro-1,3,5-triazine and benzidine as starting materials in the presence of SBA-15 as a template. Copper nanoparticles were then loaded on the C–N material to achieve a novel nanocomposite catalyst (Cu NPs-OMCN). The nanocomposite was utilized as a highly efficient catalyst for homo- and cross-coupling of terminal alkynes under base-free conditions in ethanol, and various symmetrical and unsymmetrical 1,3-diynes were obtained with good to excellent yields. Moreover, based on this reaction, a one-pot approach to synthesize 2,5-disubstituted thiophenes and furans from terminal alkynes were developed. Furthermore, the heterogeneous catalyst could be recovered and reused conveniently for several times with satisfactory yields.

A 1, 3 - butadiyne synthetic method of compound

The invention discloses a synthesis method of a 1,3-butadiyne compound and belongs to the technical field of oxidative coupling reaction of an end group alkyne compound. The synthesis method disclosed by the invention is characterized by comprising the st

Recyclable Cu/C3N4 composite catalysed homo- and cross-coupling of terminal alkynes under mild conditions

A Cu/C3N4 composite was prepared and utilized as a highly efficient and environmentally friendly catalyst for the homo- & cross-coupling of terminal alkynes. Excellent functional group tolerance and good yields were observed with oxygen as an oxidant in an isopropanol solution (or as additive) under ambient conditions. Furthermore, the composite catalyst shows good recyclability and can be recovered simply and reused several times without significant loss in its catalytic activities.

Cu(II)-CMC: A mild, efficient and recyclable catalyst for the oxidative alkyne homocoupling reaction

Cu(II) heterogenized on sodium carboxymethyl cellulose (Na-CMC) has been thoroughly characterized by different techniques. Cu(II)-CMC has been applied for the first time in the homocoupling reaction of a variety of terminal alkynes. The catalyst furnished

Copper (II) carboxymethyl cellulose base alkyne class catalytic end of synthesis of compounds 1, 3 - butadiyne compounds

The invention discloses a method for synthesizing a 1,3-butadiyne compound by copper (II) carboxymethylcellulose catalysis of a terminal alkyne compound. The technical scheme comprise the following main points: successively adding a terminal alkyne compou

Copper porphyrin-catalyzed aerobic oxidative coupling of terminal alkynes with high TON

Copper porphyrin-catalyzed Glaser-Hay-type couplings of terminal alkynes generating 1,3-diynes are described. This reaction features high TON (up to 950) and is complete in an hour, providing a facile, clean, and efficient protocol to access various 1,3-d