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41Author    R. Minkwitz, H. Prenzel, H. PritzkowRequires cookie*
 Title    Beiträge zur Chemie der Schwefel-Halogenide, 17 [1] Dimethyl(methylthio)-und Dimethyl(phenylthio)sulfonium-Salze Contributions to the Chemistry of Sulfur Halides, 17 [1] Dimethyl(methylthio)-and Dimethyl(phenylthio)sulfonium Salts  
 Abstract    IR, Raman and NMR spectroscopic studies of dimethyl(methylthio)-and dimethyl(phenyl-thio)sulfonium salts (CH 3) 2 SSR + A~ (R -CH 3 , C 6 H 5 ; A = AsF 6 ~, SbCl 6 ~) are reported. The crystal structure of (CH 3) 2 SSCH 3 + AsF 6 ~ shows for the cation a conformation different from that reported for the hexachloroantimonate. 
  Reference    Z. Naturforsch. 42b, 750—755 (1987); eingegangen am 5. Dezember 1986/4. Februar 1987 
  Published    1987 
  Keywords    Thiosulfonium Salts, NMR Spectra, Crystal Structure 
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 TEI-XML for    default:Reihe_B/42/ZNB-1987-42b-0750.pdf 
 Identifier    ZNB-1987-42b-0750 
 Volume    42 
42Author    Hansjörg Grützm, H. Erbert, W. Roesky, Mathias Noltem, GeorgeM. SheldrickRequires cookie*
 Title    Substitutionsreaktionen am N-[l-Chlor-2,2,2-trifluor-l-(trifluormethyl)ethyl]-dimethyIformamidin Substitution Reactions with N -[l-Chloro-2,2,2-trifluoro-l-(trifluorom ethyl)ethyl]-dim ethylform am idine  
 Abstract    It is difficult to achieve nucleophilic attack on a carbon atom bonded on two trifluoromethyl groups. However, N-[l-chloro-2,2,2-trifluoro-l-(trifluoromethyl)ethyl]-dimethylformamidine (1) reacts readily with H20 , MeOH, EtSH and P(OM e)3 even under mild conditions to form products 2, 3, 4 and 5. The reaction between 1 and Ph2PH is complex but leads in nearly quantitative yield to N-[2,2,2-trifluoro-l-(trifluoromethyl)ethyl]-dimethylformamidinium chloride 6 which has been characterized by an X-ray structure analysis. A reaction mechanism is proposed. 
  Reference    Z. Naturforsch. 42b, 1245—1248 (1987); eingegangen am 5. Mai/27. Juni 1987 
  Published    1987 
  Keywords    MS Spectra, Fluoroorganic Compounds, NMR Spectra 
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 TEI-XML for    default:Reihe_B/42/ZNB-1987-42b-1245.pdf 
 Identifier    ZNB-1987-42b-1245 
 Volume    42 
43Author    Werner WolfsbergerRequires cookie*
 Title    Darstellung von Alkylmethylphenylphosphanen nach der Methode von Hewertson und Watson Preparation of Alkylmethylphenylphosphines by the Method of Hewertson and Watson  
 Abstract    The reaction of C 6 H 5 (CH 3)PNa with some alkyl halides in liquid ammonia was studied. The resulting phosphines were characterized by elemental analyses, NMR spectra, and by the reaction with trimethylsilyl azide giving trimethylsilylimino triorganophosphoranes. 
  Reference    Z. Naturforsch. 43b, 295—298 (1988); eingegangen am 30. November 1987 
  Published    1988 
  Keywords    Alkylmethylphenylphosphines, N-Trimethylsilylimino Triorganophosphoranes, NMR Spectra 
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 TEI-XML for    default:Reihe_B/43/ZNB-1988-43b-0295.pdf 
 Identifier    ZNB-1988-43b-0295 
 Volume    43 
44Author    Cl, Br, Rolf Minkwitz, Arnulf WernerRequires cookie*
 Title    Methyl(trifluormethyl)haIogensulfonium-Salze [ 1 ] Halogen = F, CI, Br, I Methyl(trifluoromethyl)halosulfonium Salts [1]  
 Abstract    The preparation and spectroscopic characterization of the halosulfonium salts CH ,(CF,)SHal + A (Hal = F, Cl, Br, I, A" = AsF 6 ~~, SbF 6 ~, SbCl A ") is reported. The compounds are synthesized by the reaction of the sulfane CH,SCF, with XeF + MF h ~, Cl.F+AsFf,", Cl 2 /AsF 5 , Cl 2 /SbCl 5 , Br : /AsF 5 , or I 3 + MF 6 ~ (M = As, Sb), resp., at low temperatures. 
  Reference    Z. Naturforsch. 43b, 403—411 (1988); eingegangen am 10. Dezember 1987 
  Published    1988 
  Keywords    Preparation Raman Spectra, NMR Spectra, IR Spectra 
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 TEI-XML for    default:Reihe_B/43/ZNB-1988-43b-0403.pdf 
 Identifier    ZNB-1988-43b-0403 
 Volume    43 
45Author    Rolf Minkwitz, Andreas LiedtkeRequires cookie*
 Title    Darstellung und spektroskopische Charakterisierung von FIuor(trifluormethylsulfenyl)phosphonium-Salzen, CF 3 SPH 2 F + MF 6 -(M = As, Sb) Preparations and Spectroscopic Characterization of Fluoro(trifluoromethylsulfenyl)phosphonium Salts, CF 3 SPH 2 F~MF 6 ~ (M = As, Sb)  
 Abstract    The preparations of the title compounds are reported. The species have been characterized by multinuclear ('H, l3 C, 19 F, 3I P) NMR techniques. Their decomposition, leading mainly to PH 2 F 2 + MF 6 ~, was also studied. The Raman spectrum of CF,SPH 2 F + AsF 6 ~ is presented. 
  Reference    Z. Naturforsch. 43b, 1263—1267 (1988); eingegangen am 1. Juni 1988 
  Published    1988 
  Keywords    Fluoro(trifluoromethylsulfenyl)phosphonium Salts, NMR Spectra, Raman Spectra 
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 TEI-XML for    default:Reihe_B/43/ZNB-1988-43b-1263.pdf 
 Identifier    ZNB-1988-43b-1263 
 Volume    43 
46Author    Rolf Minkwitz, V. Olker, Gerhard, ThomasN. OrkatRequires cookie*
 Title    Darstellung und spektroskopische Charakterisierung von primären und sekundären Sulfoniumsalzen [1] Preparation and Spectroscopic Characterization of Primary and Secondary Sulfonium Salts [1]  
 Abstract    The preparation and spectroscopic characterization of the sulfonium salts R 2S H f M F6 and R SH 2+MF6~ (R = C H 3, r-C4H 9; M = As, Sb) is reported. The com pounds are synthesized by protonation of the corresponding sulfanes in the superacid system H F/M F5. 
  Reference    Z. Naturforsch. 44b, 1337—1342 (1989); eingegangen am 7. Juni 1989 
  Published    1989 
  Keywords    P reparation, Raman Spectra, NMR Spectra 
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 TEI-XML for    default:Reihe_B/44/ZNB-1989-44b-1337.pdf 
 Identifier    ZNB-1989-44b-1337 
 Volume    44 
47Author    G. Alina, S. Z. Aitseva11 ', SergeyS K Arlova, ElenaS A Lekseyevaa, LeonidA A Slanova, EvgeniV A Vtom Onovb, JörgL. OrberthbRequires cookie*
 Title    -Allylgermatrane. Synthesis, Structure and Reaction with Diazomethane  
 Abstract    Reaction of allyltribromogermane (2), readily available from dibrom o(l,4-dioxane)ger-manium(II) (1) and allylbromide, with tris(2-tributylstannoxyethyl)-amine (4) gives 1-allylgermatrane (3) in almost quantitative yield. 3 crystallizes from /7-pentane as a colourless crystalline solid which was characterized by 'H and ,3C NMR spectroscopy and by an X-ray crystal structure study. The "atrane" skeleton shows a strong conformational disorder; the Ge-N distance of 2.208(3) A suggests the presence of a coordinative Ge-N bond. Treatment of 1 -allylgermatrane (3) with CH2N2 in the presence of catalytic amounts of Pd(OAc)2 affords 1-cyclopropylmethylgermatrane (5) in high yield. 
  Reference    (Z. Naturforsch. 52b, 30—34 [1997]; received August 16 1996) 
  Published    1997 
  Keywords    Germanium, Germatrane, Cyclopropanation, X-Ray, NMR Spectra 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0030.pdf 
 Identifier    ZNB-1997-52b-0030 
 Volume    52 
48Author    Ralf Steudel, Monika Kustos, Andreas PrenzelRequires cookie*
 Abstract    y n t h e s is a n d S t r u c t u r e o f B i s [ d i(m e t h y lc y c lo p e n t a d ie n y l) c h lo r o -t it a n iu m ] t r is u lf id e [ (C p 2 C lT i)2S 3 ] -a R e a g e n t fo r T r is u lf id e L ig a n d T r a n s f e r R e a c t io n s [1] The dinuclear metallacycle of [Cp2Ti(/z-S2)2TiCp2] reacts with phosgene or thiophosgene to give [(CP2CITO2S3] which has been characterized by 1H and l3C NMR spectra as well as by an X-ray structure analysis. The trisulfido complex contains a helical TiSSSTi unit and may serve as an S3 transfer reagent in reactions with SCl-functional compounds. 
  Reference    (Z. Naturforsch. 52b, 79—82 [1997]; received June 18 1996) 
  Published    1997 
  Keywords    Titanocene Complexes, Polysulfide Ligands, Structure, NMR Spectra 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0079.pdf 
 Identifier    ZNB-1997-52b-0079 
 Volume    52 
49Author    R. Olf, M. Inkwitz, Jens JakobRequires cookie*
 Title    D arstellung und spektroskopische Charakterisierung von T rifluorm ethylazosulfonylm ethan C H 3S ( 0 ) 2N N C F 3 P rep aratio n and Spectroscopic C haracterization of Trifluorom ethylazosulfonylm ethane C H 3S ( 0 ) 2N N C F  
 Abstract    The reaction of trifluoronitrosomethane with CH3S (0)2NH2 and Na2C 0 3 as a base in THF gi­ ves the yellow liquid CH3S (0)2NNCF3, m.p. 18 °C, which was characterized by vibrational and NMR spectra. 
  Reference    Z. Naturforsch. 52b, 135—137 (1997); eingegangen am 21. Oktober 1996 
  Published    1997 
  Keywords    Trifluoromethylazosulfonylmethane, Preparation, Vibrational Spectra, NMR Spectra 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0135_n.pdf 
 Identifier    ZNB-1997-52b-0135_n 
 Volume    52 
50Author    LuRequires cookie*
 Title    Synthesis of N,C,C-Trilithio-2,5-diaIlyl- pyrrole and its Solvent-Controlled Reactions with Electrophiles  
 Abstract    te d so lu tio n s ca n b e co o led to -80 °C w ith o u t p rec ip ita tio n . B e rn d W ra c k m e y e r5 5 B e rn d Schw arze Iris O rd u n g , 2,5-Diallylpyrrole 1 reacts with an excess of "BuLi in hexane/diethylether to give the N,C,C-trilithio reagent 2. 7Li NMR spectra of 2 in THF/ HMPTA at low tem perature indicate the pres­ ence of an ionic species. Reactions of 2 in TH F with electrophiles such as H 20 , D20 , Mel, Me3SiCl and Me3SnCl lead selectively to the cis-isomers 3a -6 a, whereas the analogous reactions in hexane or diethylether afford mixtures contain­ ing both cis-and rram-isomers (e.g. 3b). 
  Reference    Z. Naturforsch. 52b, 427—430 (1997); received November 5 1996 
  Published    1997 
  Keywords    Pyrrole, Solvent Controlled Reactions, NMR Spectra 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0427_n.pdf 
 Identifier    ZNB-1997-52b-0427_n 
 Volume    52 
51Author    S.Requires cookie*
 Title    Silaheterocyclen, XXXIII [1, 2]: Cycloadditions-Reaktionen des 1.1-Dichlor-2-neopentyIsilaethens mit Pentafulvenen  
 Abstract    ilaheterocycles, X X X III [1, 2]: C y c lo a d d itio n R e a c tio n s of 1 .1 -D ic h lo ro -2 -n eo p e n ty lsilen e w ith P e n ta fu lv e n e s N o rb e rt A u n er* , C la u s-R ü d ig e r H e ik e n w ä ld e r The reaction between in situ formed l,l-dichloro-2-neopentyl-l-silene, Cl2Si=CHCH2rBu (2), and 1,1-dimethylpentafulvene (5) leads to the formation of exo/endo-isomeric [4+2] cy-cloadducts 9 and [2+2] stereoisom ers 10 in good yields. NMR spectroscopic investigations of the product mixture prove the different modes of the silene cycloaddition reactions ([4+2] vs [2+2] addition). Treatment of 9 and 10 with LiA lH 4 and LiMe yield the stereo-and regioisomeric derivati­ ves (LiAlH 4: 16. 17; MeLi: 18, 19), whereas PhMgBr reacts with 10 to give only the mono substitution, the [4+2] com pound 20, and the diphenylated silacyclobutane 21. The reactions of silene 2 with pentafulvenes 6 -8 lead to similar results. 
  Reference    Z. Naturforsch. 52b, 500—514 (1997); eingegangen am 19. Dezember 1996 
  Published    1997 
  Keywords    Cycloaddition Reactions, Neopentylsilene, Pentafulvenes, NMR Spectra 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0500.pdf 
 Identifier    ZNB-1997-52b-0500 
 Volume    52 
52Author    Bernd Wrackmeyer, Jürgen WeidingerRequires cookie*
 Title    N-Boryl-Substituted Bis(amino)stannylenes and -plumbylenes  
 Abstract    Two equivalents of N-lithio-N-trimethylsilyl-amino-9-borabicyclo[3.3.1]nonane (1) react with tin and lead dichloride by salt elimination to give the corresponding bis(amino)stannylene 2 and -plumbylene 3, respectively. The compounds 2 and 3 are monomers in solution and were characterized by 'H , i3C, 14N, 29Si, ll9Sn and 207Pb NMR spectroscopy. 
  Reference    Z. Naturforsch. 52b, 947—950 (1997); received May 22 1997 
  Published    1997 
  Keywords    Boron, Tin, Lead, Metal Amides, NMR Spectra 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0947.pdf 
 Identifier    ZNB-1997-52b-0947 
 Volume    52 
53Author    Max Herberhold, Volker Tröbs, Hong Zhou, Bernd WrackmeyerRequires cookie*
 Title    Reactivity and NMR Spectroscopic Properties of Tri(terf-butyl)plumbyl-amine  
 Abstract    Tri(rm-butyl)plumbyl-amine 1 was prepared and studied by one-(ID) and two-dimensional (2D) 'H, i3C, 5N and 207Pb NMR which allowed determination of the coupling signs /(Pb,13C) (> 0), 2y(207P b,'3C) (> 0), '7(207Pb,15N) (> 0; reduced coupling constant 1 A^(207Pb,I5N) < 0) and 27(207Pb-N-'H) (< 0). Transamination of 1 with aniline and pyrazole afforded the corresponding aniline (2) and pyrazole derivatives (3), respectively. N-Lithiation of 1, followed by treatment with Me3SiCl gave the tri(rm-butyl)plumbyl-trimethylsilyl-amine 5. The multinuclear magnetic resonance data of 2, 3 and 5 are presented. Trimethylplumbyl-phenyl-amine and trimethylplumbyl-ter/-butyl(dimethyl)silyl-amine were prepared and their NMR data were measured for comparison. 
  Reference    Z. Naturforsch. 52b, 1181—1184 (1997); received July 14 1997 
  Published    1997 
  Keywords    Lead, Organolead-nitrogen Compounds, NMR Spectra, Coupling Constants 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-1181.pdf 
 Identifier    ZNB-1997-52b-1181 
 Volume    52 
54Author    Josef Hahn, Marianne Baudler, Carl Krüger, Yi-Hung TsayRequires cookie*
 Title    Beiträge zur Chemie des Phosphors, 116 [1] Kernresonanzspektren und Kristallstruktur von Tri -tert-butyl -cy clotriphosphan Contributions to the Chemistry of Phosphorus, 116 [1] NMR Spectra and Crystal Structure of Tri-terf-butylcyclotriphosphane  
  Reference    Z. Naturforsch. 37b, 797—805 (1982); eingegangen am 1. März 1982 
  Published    1982 
  Keywords    Tri-ier^-butylcyclotriphosphane, Threo-Membered Ring Compounds, NMR Spectra, Crystal Structure 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-0797.pdf 
 Identifier    ZNB-1982-37b-0797 
 Volume    37 
55Author    Rüdiger Thamm, Ekkehard FluckRequires cookie*
 Title    Kohlensäureesterphosphide -Synthese und Cyclisierungsreaktionen Carbonic Ester Phosphides -Synthesis and Cyclization Reactions  
 Abstract    Carbonic ester phosphides, RPHCOOR' and RP(COOR')2, have been prepared by the reaction of C1COOR' with primary phosphines RPH2 in the presence of K2CO3. Some compounds of RPHCOOR' series are transformed into P-heterocycles through addition of the P-H group to the C = C doubleboncl systems. The 31 P NMR data, IR and mass spectra of the novel compounds are presented and discussed. 
  Reference    Z. Naturforsch. 37b, 965—974 (1982); eingegangen am 8. März 1982 
  Published    1982 
  Keywords    Carbonic Ester Phosphides, Mass Spectra, IR Spectra, NMR Spectra 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-0965.pdf 
 Identifier    ZNB-1982-37b-0965 
 Volume    37 
56Author    Rudolf Allmann, Eberhard Hohaus, Stanislaw 01ejnikRequires cookie*
 Title    Boron Chelates and Boron-Metal Chelates, X [1] 3-(2-Hydroxyphenyl)-2,2-diphenyl-l-oxa-3-azonia-2-borata-naphthalene- methanol (1/1): Synthesis, Spectroscopic Investigations and Crystal Structure  
 Abstract    2-Aminophenol, salicylaldehyde and diphenylboric anhydride react in methanol to form a fluorescent, chelate-like azomethineboron compound containing methanol. The title compound, C25H20BNO2 • CH3OH, was examined by UV, IR, HI, and NMR spectroscopy as well as by thermogravimetry and X-ray structure analysis (Pbnb, a= 8.815, b= 17.309, c = 28.992 Ä, R = 5.5%). These investigations show the six-membered chelate ring (chelate A) to exist as formulated in [2] and not as a five-membered chelate ring B. One methanol molecule connects two chelate molecules by hydrogen bonds, resulting in an overall ratio of chelate to methanol of 1 : 1. 
  Reference    Z. Naturforsch. 37b, 1450—1455 (1982); received May 1 O/June 11 1982 
  Published    1982 
  Keywords    Boron Chelate, Azomethine, Crystal Structure, UV Spectra, NMR Spectra 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-1450.pdf 
 Identifier    ZNB-1982-37b-1450 
 Volume    37 
57Author    Wilfried Peters, Gerhard HageleRequires cookie*
 Title    Kernresonanzspektroskopische Untersuchungen an Organophosphorverbindungen - Thiophosphorylbromide RR P(S)Br: R,R =CH3, C2H5, f-C3H7, t-C4H9 NMR Studies on Organophosphorous Compounds -Thiophosphorylbromides RR'P(S)Br  
 Abstract    NMR spectra of dialkylthiophosphoryl bromides RR'P(S)Br are analyzed. Methods are demonstrated for C2H5(t-C3H7)P(S)Br. A correlation between <53ip in the 31 P NMR spectra and the number of y3-methyl groups is discussed. 
  Reference    (Z. Naturforsch. 38b, 96—102 [1983]; eingegangen am 23. August 1982) 
  Published    1983 
  Keywords    Dialkylthiophosphoryl Bromides, NMR Spectra, X H NMR Spectra, 31 P NMR Spectra 
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 TEI-XML for    default:Reihe_B/38/ZNB-1983-38b-0096.pdf 
 Identifier    ZNB-1983-38b-0096 
 Volume    38 
58Author    S. V. Verkhovskii, B. Z. Malkin, A. Trokiner, A. Yakubovskii, E. Hallet, A. Ananyev, A. Gerashenko, Yu Piskunov, S. Saikin, A. Tikhomirov, V. OzhoginRequires cookie*
 Title    Quadrupole Effects on 73 Ge NMR Spectra in Isotopically Controlled Ge Single Crystals  
 Abstract    NMR spectra of 73 Ge (nuclear spin / = 9/2) in perfect single crystals of germanium with different isotopic content were measured at 80, 300, and 450 K. The observed specific line shapes gave evidence of the isotopic disorder, in particular, abnormal broadening of the spectrum was found for the magnetic field directed along the [111] axis. Local lattice deformations in the germanium crystal lattice due to "isotopic disorder" were calculated in the framework of the adiabatic bond charge model. The results were applied to study random non-cubic crystal field interactions with the nuclear quadrupole moments and corresponding effects on NMR spectra. The simulated second moment of the resonance frequency distributions caused by the magnetic dipole-dipole and electric quadrupole interactions are used to analyze the lineshapes, theoretical predictions being in a qualitative agreement with the experimental data. 
  Reference    Z. Naturforsch. 55a, 105—110 (2000); received September 11 1999 
  Published    2000 
  Keywords    Isotopic Disorder, Ge Single Crystal, NMR Spectra, Quadrupole Effects 
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 TEI-XML for    default:Reihe_A/55/ZNA-2000-55a-0105.pdf 
 Identifier    ZNA-2000-55a-0105 
 Volume    55 
59Author    Ekkehard Lindner, Claus-Peter Krieg, Sigurd Hoehne, Axel RauRequires cookie*
 Title    Darstellung und Eigenschaften von und Reaktionen mit metallhaltigen Heterocyclen, XXTTT [1] Untersuchungen zur P=S-heteroanalogen Cyclocotrimerisierung von Alkinen mit Nitrilen bzw. Isocyaniden Preparation and Properties of, and Reactions with, Metal-Containing Heterocycles, XXIII [1] Investigations on P=S-Heteroanalogous Cyclocotrimerization of Alkynes with Nitriles and Isocyanides, Respectively  
 Abstract    Structure of [(OC)4MnSP(CH 3)2]2, The dimanganadiphosphadithiacyclohexadiene [(OC)4MnSP(CH 3)2]2 (1) crystallizes in the H,C CH, \ / 3 / P =\ (OC).Mn Mn(CO), * \ / S=P /\ HjC CHj 1 /-PC CH * (OC)tMn I CH, * L Y\ CH, (OCULMn | CHj . CO \ ^ C" \R' L \ t-Bu C6H" C6H5 R'NC a b c PR'3 d R = C02CHJ 3a-d orthorhombic space group Pbca with Z = 4. Attempts to cyclotrimerize the intermediate 
  Reference    Z. Naturforsch. 36b, 1487—1492 (1981); eingegangen am 28. Juli 1981 
  Published    1981 
  Keywords    Isocyanide Complexes of Heteromanganacyclopentadienes, Mass Spectra, IR Spectra, NMR Spectra 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-1487.pdf 
 Identifier    ZNB-1981-36b-1487 
 Volume    36 
60Author    Ertugrul Arpac, Lutz DahlenburgRequires cookie*
 Title    Oligophosphin-Liganden, I  
 Abstract    Einfache Synthesen der trimethylenverknüpften Triphosphine RP[(CH2)3PPh2]2 und ihrer Vorstufen Ph2P(CH2)3P(H)R (R Ph, Me) Oligophosphine Ligands, I Convenient Syntheses of the Trimethylene-linked Triphosphines RP[(CH2)3PPh2]2 and their Precursors Ph2P(CH2)3P(H)R (R = Ph, Me) The secondary-tertiary diphosphines Ph2P(CH2)3P(H)Ph (2) and Ph2P(CH2)3P(H)Me (3) have been prepared from Ph2P(CH2)3Cl (1) and NaP(H)Ph or LiP(H)Me, respectively. Metallation of 2 and 3 with n-butyl lithium and further reaction of the lithio-derivatives with one equivalent of 1 yields PhP[(CH2)3PPh2]2 (4) and MeP[(CH2)3PPh2]2 (5). The tritertiary phosphines 4 and 5 have likewise been obtained from RPLi2 (R = Ph, Me) and two equivalents of 1. The synthesis of 4 from PhPCl2 and two equivalents of the Grignard reagent of 1 is also reported. Each of the phosphines 1-5 was characterized by NMR and mass spectroscopy. 
  Reference    Z. Naturforsch. 35b, 146—152 (1980); eingegangen am 26. Oktober 1979 
  Published    1980 
  Keywords    Secondary-tertiary Diphosphines, Tritertiary Phosphines, Preparation, NMR Spectra, Mass Spectra 
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 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0146.pdf 
 Identifier    ZNB-1980-35b-0146 
 Volume    35