Relevant bibliographies by topics / Cumulenones

Academic literature on the topic 'Cumulenones'

Author: Grafiati
Published: 10 December 2022
Last updated: 29 January 2023

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Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Cumulenones.'

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Journal articles on the topic "Cumulenones"

1

Ichikawa, Hiroshi, and Yukiko Ebisawa. "Concerning Bent Structures of Cumulenones." Bulletin of the Chemical Society of Japan 58, no. 10 (October 1985): 3025–26. http://dx.doi.org/10.1246/bcsj.58.3025.

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2

Nguyen, Quynh L. D., William K. Peters, and Ryan C. Fortenberry. "Highly-excited state properties of cumulenone chlorides in the vacuum-ultraviolet." Physical Chemistry Chemical Physics 22, no. 21 (2020): 11838–49. http://dx.doi.org/10.1039/d0cp01835j.

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A detailed understanding of VUV-driven photochemistry in complex organic molecules is challenging. This quantum chemical analysis reports the electronic properties and ionization energies up to the VUV range (6–11 eV) of the chlorinated cumulenones.
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3

East, Allan L. L. "The kinkiness of cumulenones: H2C3O, H2C4O, and H2C5O." Journal of Chemical Physics 108, no. 9 (March 1998): 3574–84. http://dx.doi.org/10.1063/1.475752.

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4

Liang, Congxin, and Leland C. Allen. "Double bond deformation: cumulenes, cumulenones, and Group IV ethylene analogs." Journal of the American Chemical Society 113, no. 6 (March 1991): 1873–78. http://dx.doi.org/10.1021/ja00006a001.

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5

Wang, Erjuan, Xiaoping Fu, Xin Xie, Jingjin Chen, Hongjun Gao, and Yuanhong Liu. "Gold and Brønsted acid catalyzed isomerization of [3]cumulenols and [3]cumulenones: efficient syntheses of 1,5-dien-3-ynes and furan derivatives." Tetrahedron Letters 52, no. 16 (April 2011): 1968–72. http://dx.doi.org/10.1016/j.tetlet.2011.02.057.

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6

LIANG, C., and L. C. ALLEN. "ChemInform Abstract: Double Bond Deformation: Cumulenes, Cumulenones, and Group IV Ethylene Analogues." ChemInform 22, no. 28 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199128041.

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Wang, Erjuan, Xiaoping Fu, Xin Xie, Jingjin Chen, Hongjun Gao, and Yuanhong Liu. "ChemInform Abstract: Gold and Broensted Acid Catalyzed Isomerization of [3]Cumulenols and [3]Cumulenones: Efficient Syntheses of 1,5-Dien-3-ynes and Furan Derivatives." ChemInform 42, no. 29 (June 27, 2011): no. http://dx.doi.org/10.1002/chin.201129058.

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8

McCarthy, Michael C., Luyao Zou, and Marie-Aline Martin-Drumel. "To kink or not: A search for long-chain cumulenones using microwave spectral taxonomy." Journal of Chemical Physics 146, no. 15 (April 21, 2017): 154301. http://dx.doi.org/10.1063/1.4981125.

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9

Scott, A. P., and L. Radom. "Are cumulenones kinked? A systematic high-level ab initio study of H 2 CCCO, H 2 CCCCO and H 2 CCCCCO." Journal of Molecular Structure 556, no. 1-3 (December 2000): 253–61. http://dx.doi.org/10.1016/s0022-2860(00)00640-2.

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10

Fu, Xiaoping, Jingjin Chen, Guangyu Li, and Yuanhong Liu. "Diverse Reactivity of Zirconacyclocumulenes Derived from Coupling of Benzynezirconocenes with 1,3-Butadiynes towards Acyl Cyanides: Synthesis of Indeno[2,1-b]pyrroles or [3]Cumulenones." Angewandte Chemie International Edition 48, no. 30 (July 13, 2009): 5500–5504. http://dx.doi.org/10.1002/anie.200900951.

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Dissertations / Theses on the topic "Cumulenones"

1

Das, Neves Nicolas. "Synthèse et réactivité de [3]-cumulenols." Paris 6, 2011. http://www.theses.fr/2011PA066703.

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Abstract:
Le travail décrit dans ce manuscrit porte sur la synthèse de [3]-cumulènes par voie radicalaire et la réactivité des alcools [3]-cumuléniques. La première partie détaille nos différentes tentatives d’accès aux [3]-cumulènes par voie radicalaire. Si différents systèmes ont été utilisés, aucun d’entre eux n’a permis l’obtention des composés attendus. La seconde partie décrit la réactivité des alcools [3]-cumuléniques en catalyse organométallique. Lorsqu’une catalyse à l’or ou à l’argent est utilisée, un furane et un vinyl furane sont majoritairement isolés. Leurs proportions peuvent être modulées suivant la concentration et le métal utilisé. Un mécanisme est proposé pour la formation de ces deux produits. Enfin, les catalyses au fer et au palladium ont été utilisées soit pour la formation de vinyl furane soit pour réaliser une séquence domino de cyclisation-allylation et accéder à des motifs furaniques complètement substitués
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Conference papers on the topic "Cumulenones"

1

McCarthy, Michael, and Marie-Aline Martin-Drumel. "TO KINK OR NOT: THE SEARCH FOR LONG CHAIN CUMULENONES USING MICROWAVE SPECTRAL TAXONOMY." In 71st International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.rj01.

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2

Lee, Kelvin, John Stanton, and Michael McCarthy. "ON THE RELATIVE STABILITY OF CUMULENONE AND ALDEHYDE ISOMERS: WHEN WE HEAT345(Q) THINGS UP." In 72nd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2017. http://dx.doi.org/10.15278/isms.2017.wf10.

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You might also be interested in the extended bibliographies on the topic 'Cumulenones' for particular source types:
Journal articles
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