Výsledky vyhledávání - "Johannes Kadel"

ChemInform Abstract: Structure of Trimethyltantalum Difluoride, (CH3)3TaF2

Publikováno v: ChemInform. 25

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::047f8644f5863add762e15b9951ebb35
https://doi.org/10.1002/chin.199447033

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An unusual relationship between the nitrogen-fluorine bond lengths and force constants in N-fluoroamines

Autor: Heinz Oberhammer, Hans Georg Mack, Dines Christen, O. D. Gupta, Jean'ne M. Shreeve, Johannes Kadel, Robert L. Kirchmeier

Publikováno v: Journal of the American Chemical Society. 113:9131-9135

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7013e507109279a9a52d6e5f5b7589bf
https://doi.org/10.1021/ja00024a016

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Chemistry of sulfur-halogen compounds. 37. Synthesis of CF3SSI, vibrational analyses for (trifluoromethyl)disulfanes CF3SSX (X = F, Cl, Br, I, and H), and gas-phase structures of CF3SSF and CF3SSH

Autor: Heinz Oberhammer, Johannes Kadel, Rolf Minkwitz, Reinhard Lekies, Juergen Sawatzki, Dirk Lennhoff

Publikováno v: Inorganic Chemistry. 29:2587-2590

Valence force fields for these (trifluoromethyl)disulfanes were derived from the spectral data. The S-S force constant for X=Cl, Br, and I is equal to that in S 8 . The S-X force constants decrease steadily with increasing size of the halogen. Furthe

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https://doi.org/10.1021/ic00339a012

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Structure of Trimethyltantalum Difluoride, (CH3)3TaF2

Autor: Heinz Oberhammer, Johannes Kadel

Publikováno v: Inorganic Chemistry. 33:3197-3198

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2c57befea1a5ddb2f1a7f324b76e5b61
https://doi.org/10.1021/ic00092a032

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Triazaphosphinine – Reaktionen, Zwitterionen, P–B-Austausch/ Triazaphosphinines – Reactions, Zwitter Ions, P – B-Exchange

Autor: Johannes Kadel, Matthias Meyer, Heinz Oberhammer

Publikováno v: Zeitschrift für Naturforschung B. 43:1010-1016

2,2-Dichloro-triazaphosphinine (2) reacts with SbF3 in the molar ratio 3:1 to give the mixed halogenated triazaphosphinine (3). New addition compounds 5 and 6 can be formed in the reaction of the zwitter ion 4 and amines or in the reaction of 2.2-dif

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::781f5bf8665e89a425a7004c31a0b2f0
https://doi.org/10.1515/znb-1988-0816

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