Polymerization of acetylene: polyynes, but not carbyne‡

Literature Information

Publication Date 2016-11-08
DOI 10.1039/C6QO00648E
Impact Factor 5.281
Authors

Dominik Prenzel, Rolf W. Kirschbaum, Wesley A. Chalifoux, Robert McDonald, Michael J. Ferguson, Thomas Drewello


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Abstract

The formation of polyynes via polymerization of acetylene gas and endcapping with the tris(3,5-di-t-butylphenyl)methyl moiety (Tr*, supertrityl) has been explored. The polymerization process has been optimized based on the length of the polyyne endcapping groups. Separation-purification-identification has been achieved through reversed-phase (RP) high performance liquid chromatography (HPLC), utilizing UV-vis detection, which offers UV-vis spectra of the polyyne products. The chain length of individual polyynes can then be established through comparison to the spectra trends of known polyyne samples. LDI and MALDI mass spectrometry is used to examine the presence of Tr*[n] polyynes in the crude reaction mixture. The combined analyses show that polymerization reactions of acetylene using the supertrityl endgroup allow formation of polyynes, but much shorter than could be achieved by stepwise syntheses.

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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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