| 81 | Author
| Gernot Heckmann, Ekkehard Fluck, Peter Kuhm | Requires cookie* | | Title
| A [l,3,4]Thiazaphospholidine, Preparation and NMR Data  | | | Abstract
| Preparation and properties of a [l,3,4]thiaza-phospholidine are described. The 31 P. 13 C and 'H NMR spectra in double and triple resonance mode are recorded and discussed in detail. | | |
Reference
| (Z. Naturforsch. 42b, 115—117 [1987]; eingegangen am 29. August 1986) | | |
Published
| 1987 | | |
Keywords
| [l, 3, 4]Thiazaphospholidine, NMR Spectra, Triple Resonance | | |
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| default:Reihe_B/42/ZNB-1987-42b-0115_n.pdf | | | Identifier
| ZNB-1987-42b-0115_n | | | Volume
| 42 | |
83 | Author
| Lothar Weber, Georg Meine | Requires cookie* | | Title
| Zur Reaktivität von Diphosphenylkomplexen des Eisens und Rutheniums gegenüber Tetracarbonylnickel Transition Metal Substituted Diphosphenes, VI [1] On the Reactivity of Diphosphenyl Complexes of Iron and Ruthenium towards Tetracarbonyl Nickel  | | | Abstract
| The diphosphenyl complexes (?/ 5 -CsMe0(CO 2)M-P = P-Ar (8) (M = Fe, Ru; Ar = 2,4,6-rm-BU,C 6 H 2) react with excess Ni(CO) 4 to yield the adducts (77 5 -C 5 Me 5)(CO) 2 M[Ni(CO) 3 ]P=PAr (9). The products have been characterized by elemental analysis as well as by spectroscopic data (IR. 'H, 13 C, 31 P NMR). | | |
Reference
| Z. Naturforsch. 42b, 774—776 (1987); eingegangen am 26. Januar 1987 | | |
Published
| 1987 | | |
Keywords
| Metal Substituted Diphosphenes, Tetracarbonyl Nickel, NMR Spectra, IR Spectra | | |
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| default:Reihe_B/42/ZNB-1987-42b-0774.pdf | | | Identifier
| ZNB-1987-42b-0774 | | | Volume
| 42 | |
84 | Author
| Jörg Apitz, Joseph Grobe, Due Le Van | Requires cookie* | | Title
| Darstellung und [l+4]-Cycloaddition von Methylthio-chlorophosphanen RP(Cl)SMe (R = Me, Et, Ph) Preparation and [l+4]-Cycloaddition of Methylthio-chlorophosphanes RP(Cl)SMe (R = Me, Et, Ph)  | | | Abstract
| The methylthio-chlorophosphanes RP(Cl)SMe [R = Me (1). Et (2). Ph (3)] are prepared in good yields (62—65%) by condensation reactions of the corresponding dichlorophosphanes RPC12 with methanethiol in the presence of trimethylamine (molar ratio 1:1:1). 1 and 3 have been used to produce 3-phospholene sulfides in a one-pot process by reaction with 1,3-dienes at 70 to 100 °C. Reaction proceeds via [1 +4]-cycloadducts, which in suitable cases can be isolated and used for the preparation of the corresponding 3-phospholene oxides. New compounds were characterized by elemental analysis and spectroscopic investigations (NMR. MS). | | |
Reference
| Z. Naturforsch. 43b, 257—260 (1988); eingegangen am 30. November 1987 | | |
Published
| 1988 | | |
Keywords
| Methylthio-chlorophosphanes, 3-Phospholene Sulfides and Oxides Mass Spectra, NMR Spectra | | |
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| default:Reihe_B/43/ZNB-1988-43b-0257.pdf | | | Identifier
| ZNB-1988-43b-0257 | | | Volume
| 43 | |
85 | Author
| Ekkehard Fluck, Peter Kuhm, Heinz Riffel | Requires cookie* | | Title
| [l,4,2]Diazaphospholidine [l,4,2]Diazaphospholidines  | | | Abstract
| Bis(diethylamino)phosphanylacetylen reacts with N.N'-dimethyl thiourea to give 2-diethyl-amino-l,4-dimethyl-3-methylene-[l,4,2]diazaphospholidine-5-thion (2) besides the [1.3.4]thi-azaphospholidine (1). The latter compound is converted into 2 by heating. Reaction of 2 with various reagents yields other members of the title compound class. All new compounds are characterized by some reactions and their NMR and IR spectra. In addition, the results of an X-ray structure analysis of 2-diethylamino-l ,4-dimethyl-3-methylene-2-thioxo-[l ,4.2]diazaphos-pholidine-5-thion (5) are reported. | | |
Reference
| Z. Naturforsch. 43b, 1481—1489 (1988); eingegangen am 17. Mai 1988 | | |
Published
| 1988 | | |
Keywords
| [l, 4, 2]Diazaphospholidines, NMR Spectra, Crystal Structure | | |
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| default:Reihe_B/43/ZNB-1988-43b-1481.pdf | | | Identifier
| ZNB-1988-43b-1481 | | | Volume
| 43 | |
87 | Author
| Anne-Kathrin Duhme, Henry Strasdeit | Requires cookie* | | Title
| Ligandenmangelkomplexe des Cadmiums. Synthese und spektroskopische Charakterisierung molekularer (Pentafluorphenyl)cadmium-Thiolate und die Struktur des Cubankomplexes [{Cd(C6F5)(SBur)}4] Ligand-Deficient Complexes of Cadmium. Synthesis and Spectroscopic Characterization o f Molecular Pentafluorophenyl Cadmium Thiolates and the Structure o f the Cubane Complex [{Cd(C6F5)(SBuf)}4]  | | | Abstract
| In toluene, bis(pentafluorophenyl)cadmium(II) and thiols RSH (R = Bu', 2,4,6-Pr'3C6H2, 2,4,6-Bu'3C6H2) react to give soluble pentafluorophenyl cadmium thiolates [(Cd(C6F5)(SR)} J. The compounds [{Cd(C6F 5)(SBu')}4] (1)0 .5 C6H5CH3, [ {Cd(C6F5)(SC6H2Pr'3-2,4,6)} J (2)-ca. 0.25n C6H 5CH3, and [{Cd(C6F5)(SC6H2Bu'3-2,4,6)} J (3) ca. 0.25« C6H5CH3 have been prepared in 65, 59 and 78% yield, respectively. 1-0.5 C6H5CH3 crystallizes in the triclinic space group PI with a = 11,635(1)Ä, b = 11.583(1)Ä, c = 21.480(2)Ä, a = 82.12(1)°, ß = 76.26(1)°, y — 89.35(1)°, and Z = 2. 1 is a cubane-type complex with a {Cd4(/z3-SBur)4}4+ core. Each Cd atom is coordinated by three bridging thiolato ligands and one terminal C6F5 group (C d -S 2.62 A, C d -C 2.15Ä (mean values)). The central C atoms of the Bu'S" ligands of 1 show a remarkable low-field shift o f their 13C N M R resonance (12.3 ppm relative to the value of the free thiol). A characteristic spectral feature of (Cd(C6F5) } + complexes is the large value of the coupling constant 2/ (19F ,13C) o f the ipso-C atom (1, 2: 68 Hz; 3: 67 Hz). The complexes [Cd(C6F5)(SR) + H]+, [Cd(SR)2 + H]+, and [Cd2(SR)3]+ were identified in the Cl mass spectra (/50-butane) of 2 and 3. | | |
Reference
| (Z. Naturforsch. 49b, 119—127 [1994]; eingegangen am 17. August 1993) | | |
Published
| 1994 | | |
Keywords
| Cadmium Complexes, Thiolates, Crystal Structure, NMR Spectra, Mass Spectra | | |
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| default:Reihe_B/49/ZNB-1994-49b-0119.pdf | | | Identifier
| ZNB-1994-49b-0119 | | | Volume
| 49 | |
88 | Author
| JosephG. Robe, Duc Le Van, JostW. Innemöller, Bernt Krebs, M. Echtild Läge | Requires cookie* | | Title
| Reaktive E=C(p-p)7r-Systeme, XLIII [1] Darstellung und Charakterisierung P-Phosphino-oder P-Arsino-substituierter Fluorphosphaalkene des Typs R2E-P=C(F)NEt2 (R = Me, CF3, Me2N; E = P, As)  | | | Abstract
| Reactive E=C(p-p)-7r System s XLIII [1] Synthesis and Characterization o f P -Phosphino or P-A rsino Substituted Fluoro-phosphaalkenes of the Type R 2E -P=C (F)N Et2 (R = Me, C F 3, M e7N; E = R As) The easily accessible phosphaalkene HP=C(F)NEt2 (lb) reacts with halophosphanes or -arsanes R2EX (X = Cl, I) in the presence of NEt3 to give P-phosphino-or -P-arsino sub stituted fluorophosphaalkenes of the type RiE-P=C(F)NEti (2 -6) in high yields (60 -85 %) [R2E: (CF3)2P (2), Me2N(CF3)P (3), Me2P (4), (CF3)2As (5), M e2As (6)]. The analogous re-action of ib with CF3PI2 (molar ratio 1:2) unexpectedly leads to the triphosphetene Et2N | | |
Reference
| Z. Naturforsch. 51b, 778—784 (1996); eingegangen am 30. November 1995 | | |
Published
| 1996 | | |
Keywords
| Phosphaalkenes, 1, 2, 3-Triphosphetenes, NMR Spectra, Crystal Structure | | |
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| default:Reihe_B/51/ZNB-1996-51b-0778.pdf | | | Identifier
| ZNB-1996-51b-0778 | | | Volume
| 51 | |
89 | Author
| Max Herberhold, E. Bertholdt, WolfgangM. Iliu, BerndW. Rackmeyer | Requires cookie* | | Title
| N-Functionalization of the Tetrahedrane Fe2(CO)6(/z-SNH)  | | | Abstract
| The azadiferrathia tetrahedrane, Fe2(CO)6(£/-SNH) (1), was deprotonated to give the anion [Fe2(CO)6(/J-SN)]_ (2) which reacts with halides of phosphorus, arsenic, silicon, germanium, tin and boron by formation of element-nitrosen bonds. The new compounds were characterized by their IR. N M R ('H , mB, i3C, i5N, 29S i,3 P, m S n)and mass spectra. The molecular structure of [Fe2(CO)6(A/-SN-SiMe2CH2-)]2 (11) was determined by X-ray structure analysis (space group P i; triclinic; a = 799.8(2), b = 958.5(2), c = 1035.7(2) pm, a = 86.30(2)°, (3 = 81.27(2)°, 7 = 69.90(2)°). | | |
Reference
| Z. Naturforsch. 51b, 1283—1289 (1996); received March 27 1996 | | |
Published
| 1996 | | |
Keywords
| Azadiferrathia, Tetrahedrane, Cluster Anion, Element-Nitrogen Bonds, NMR Spectra | | |
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| default:Reihe_B/51/ZNB-1996-51b-1283.pdf | | | Identifier
| ZNB-1996-51b-1283 | | | Volume
| 51 | |
90 | Author
| | Requires cookie* | | Title
|  | | | Abstract
| The reaction of trifluoromethylchlorosulfane with an excess of hydrogensulfide yields trifluoromethyldisulfane. The new compound has been characterised by its IR, Raman, 19F and NMR, UY and mass spectrum, melting and boiling point and by vapour pres sure data. The result of some chemical reactions are reported. Furthermore, previously unreported NMR and mass spectral data of CF3SH, CF3S3CF3 and CF3S4CF3 are given. | | |
Reference
| (Z. Naturforsch. 30b, 169—174 [1975]; eingegangen am 12. Dezember 1974) | | |
Published
| 1975 | | |
Keywords
| Sulfur-fluorine Chemistry, NMR Spectra, IR Spectra, Raman Spectra, Mass Spectra | | |
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| default:Reihe_B/30/ZNB-1975-30b-0169.pdf | | | Identifier
| ZNB-1975-30b-0169 | | | Volume
| 30 | |
91 | Author
| Werner Zeiss, Kleomenis Barlos, 7. ^. | Requires cookie* | | Title
| Cyclotri(/ 5 -phospliazane) Cyclotri(A 3 -phosphazanes)  | | | Abstract
| P-perhalogenated cyclotri(A 3 -phosphazanes) 3 a, b are obtained from the reaction of 1 or 2 with excess PX3 (X = Cl, Br). Under mild reaction conditions 4—7 are found to be intermediates. The existence of a six-membered ring trimer is proven by NMR and mass spectroscopy. No dimer (XPNMe)2 could be detected. Nachdem uns kürzlich die Darstellung zweier per-alkylierter Cyclo£efra(/l 3 -phosphazane) (RPNMe)4, R = Me und Et, gelang [1], berichten wir hier über am Phosphor halogensubstituierte Cyclo tri(X z -phosphazane). Die PN-Verknüpfung erfolgt dabei in an sich längst bekannter Weise [2] durch Abspal-tung von Halogensilan aus Silylamin und Halogen-phosphan. 3 a, b sind aus dem Cyclotrisilazan (1) und dem Heptamethyldisilazan (2) jeweils mit einem Über-schuß von PX3 zugänglich. (MeNSiMe2)3 • 3 PX3 1 ~--<3Me2SiX2 3 PX-; Me I X 3 (Me3Si)2NMe 2 3a, X= Cl b, X= Br Unterbricht man die Umsetzung von PX3 mit 1 nach Abklingen der exothermen Reaktion, so findet man NMR-spektroskopisch hauptsächlich die Phos-phorverbindungen 4 und 5 neben geringen Mengen längerkettiger Verbindungen. Unter milden Bedin-gungen und in Dichlormethan als Lösungsmittel ge-lingt es jeweils, 7 nachzuweisen. Me Me 1 I X2P —N-SiMe2X X2P-N —PX2 4 5 X2P-N -SiMe3 6 Me Br Me | | |
Reference
| Z. Naturforsch. 34b, 423—425 (1979); eingegangen am 9. 0ktober/20. November 1978 | | |
Published
| 1979 | | |
Keywords
| Cyclotri(A 3 -phosphazanes), Reaction Intermediates, Mass Spectra, NMR Spectra | | |
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| default:Reihe_B/34/ZNB-1979-34b-0423.pdf | | | Identifier
| ZNB-1979-34b-0423 | | | Volume
| 34 | |
95 | Author
| Othmar Stelzer, Norbert Weferling | Requires cookie* | | Title
| Reaktionen koordinierter Liganden, VI [1] Substituenteneinflüsse bei der Bildung von Tri-und Tetraphosphinen in der Koordinationssphäre von Übergangsmetallen Reactions of Coordinated Ligands, VI [1] Influence of Substituents on the Formation of Tri-and Tetraphosphines in the Coordination Sphere of Transition Metals  | | | Abstract
| The lithiumphosphido complex cis-Mo(CO)4(Me2PLi)2 reacts with dichlorophosphines RPCI2 (R = Ph, Bu') to give coordination compounds of tetraphosphines Me2P-PR-PR-PMe2, whereas the complex of the triphosphine eis -Mo (CO)4 (Ph2P-PMe-PPh2) is obtained starting with the lithiumphosphido complex cis-Mo(CO)4(Ph2PLi)2. Phenyldilithiumphosphine and the chlorophosphine complexes cis-Mo(CO)4(R2PCl)2 (R = Me, Ph) give in low yield cis-Mo(CO)4(R2P-PPh-PPh-PR2) and cis-Mo(CO)4(R2P-PPh-PR2). The mechanisms of these reactions are discussed. The {3ippjj-and { 1 H} 31 P-NMR spectra are analysed and correlated with the structures of these complexes. | | |
Reference
| (Z. Naturforsch. 35b, 74—81 [1980]; eingegangen am 13. Juni 1979) | | |
Published
| 1980 | | |
Keywords
| Lithiumphosphido Complexes, Tri-and Tetraphosphine Complexes, Halogen-Metal Exchange, NMR Spectra | | |
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| default:Reihe_B/35/ZNB-1980-35b-0074.pdf | | | Identifier
| ZNB-1980-35b-0074 | | | Volume
| 35 | |
97 | Author
| Nicholas Bodor, JamesJ. Kaminski, S. D. Worley, StevenH. Gerson, N. J. | Requires cookie* | | Title
| Quantitative Evaluation of the Reactivity of Alkylating Agents  | | | Abstract
| A sensitive and reproducible method for quantitative evaluation of the relative reactivities of alkylating agents was developed, based on competitve alkylation. The method is superior to the known colorimetric methods. The reactivities of the agents could also be correlated with the 13 C chemical shifts of the a-methylene. The method was successfully applied for the ranking of "soft" alkylating agents of low reactivity. It was recently found that "soft" alkylating RI | | |
Reference
| Z. Naturforsch. 35b, 758—763 (1980); received February 4 1980 | | |
Published
| 1980 | | |
Keywords
| Alkylating Agents, Soft Drugs, NMR Spectra, Competitive Alkylation, Soft Quaternary Salts | | |
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| default:Reihe_B/35/ZNB-1980-35b-0758.pdf | | | Identifier
| ZNB-1980-35b-0758 | | | Volume
| 35 | |
|