Foszfóniumion (Hungarian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Foszfóniumion" in Hungarian language version.

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14doi.org

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2nih.gov

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1web.archive.org

1^st place

1rhodia-proban.com

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1monash.edu

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1science.org

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doi.org

dx.doi.org

(2007) „An Acidity Scale of Tetrafluoroborate Salts of Phosphonium and Iron Hydride Compounds in [D₂]Dichloromethane”. Chem. Eur. J. 13 (13), 3796–3803. o. DOI:10.1002/chem.200601484. PMID 17245785.
H.-F. Klein. Trimethylphosphonium Methylide (Trimethyl Methylenephosphorane), Inorganic Syntheses, Inorganic Syntheses, 138–140. o.. DOI: 10.1002/9780470132494.ch23 (1978). ISBN 9780470132494
(1993) „Crystal and Molecular structure of a metastable modification of phosphorus pentachloride”. Journal of the Chemical Society, Chemical Communications (11), 957–958. o. DOI:10.1039/c39930000957.
(1990) „Measurement of pK_a Values for Phosphonium Salts via the Kinetics of Proton Transfer to an Electrogenerated Base”. Journal of the Chemical Society, Chemical Communications (9), 662. o. DOI:10.1039/C39900000662.
Leírása: (1960) „Methylenecyclohexane”. Organic Syntheses 40, 66. o. DOI:10.15227/orgsyn.040.0066.
(1978) „Nature of Phosphorus(V) Chloride in Ionizing and Nonionizing Solvents”. Journal of the American Chemical Society 95 (5), 1474–1479. o. DOI:10.1021/ja00786a021.
(1996) „An X-ray crystallorgraphic study of the reagent Ph₃PCl₂; not charge-transfer, R₃P–Cl–Cl, trigonal bipyramidal or [R₃PCl]Cl but an unusual dinuclear ionic species, [Ph₃PCl⁺⋯Cl_–⋯⁺CIPPh₃]Cl containing long Cl–Cl contacts”. Chemical Communications (22), 2521–2522. o. DOI:10.1039/CC9960002521.
(2014) „Degenerate Nucleophilic Substitution in Phosphonium Salts”. J. Am. Chem. Soc. 136 (46), 16217–16226. o. DOI:10.1021/ja507433g. PMID 25384344.
(1981) „Michaelis–Arbuzov rearrangement”. Chem. Rev. 81 (4), 415–430. o. DOI:10.1021/cr00044a004.
(2008) „Flame Retardants in Commercial Use or Development for Textiles”. J. Fire Sci. 26 (3), 243–281. o. DOI:10.1177/0734904108089485.
Svara, Jürgen; Weferling, Norbert; Hofmann, Thomas. Phosphorus Compounds, Organic, Ullmann's Encyclopedia of Industrial Chemistry. John Wiley & Sons, Inc.. DOI: 10.1002/14356007.a19_545.pub2 (2008)
(1956) „Intermediate for Flame-Resistant Polymers-Reactions of Tetrakis(hydroxymethyl)phosphonium Chloride”. Industrial and Engineering Chemistry 48 (1), 64–67. o. DOI:10.1021/ie50553a021.
Tetrahalo Oxorhenate Anions, Inorganic Syntheses, Inorganic Syntheses, 257–262. o.. DOI: 10.1002/9780470132623.ch42 (1996). ISBN 9780470132623
G. A. Wiley, R. L. Hershkowitz, B. M. Rein, B. C. Chung. „Studies in Organophosphorus Chemistry. I. Conversion of Alcohols and Phenols to Halides by Tertiary Phosphine Dihalides”. J. Am. Chem. Soc. 1964 (86 (5)), 964–965. o. DOI:10.1021/ja01059a073.

monash.edu

lens.monash.edu

Breakthrough brings green ammonia production closer to reality

nih.gov

pubmed.ncbi.nlm.nih.gov

(2007) „An Acidity Scale of Tetrafluoroborate Salts of Phosphonium and Iron Hydride Compounds in [D₂]Dichloromethane”. Chem. Eur. J. 13 (13), 3796–3803. o. DOI:10.1002/chem.200601484. PMID 17245785.
(2014) „Degenerate Nucleophilic Substitution in Phosphonium Salts”. J. Am. Chem. Soc. 136 (46), 16217–16226. o. DOI:10.1021/ja507433g. PMID 25384344.

rhodia-proban.com

Frequently asked questions: What is the PROBAN® process?. Rhodia Proban. [2012. december 7-i dátummal az eredetiből archiválva]. (Hozzáférés: 2013. február 25.)

science.org

Nitrogen reduction to ammonia at high efficiency and rates based on a phosphonium proton shuttle

web.archive.org

Frequently asked questions: What is the PROBAN® process?. Rhodia Proban. [2012. december 7-i dátummal az eredetiből archiválva]. (Hozzáférés: 2013. február 25.)