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41Author    Tristram Chivers, Masood Parvez, Peter ZoricakRequires cookie*
 Title    Preparation and X-Ray Structure of 4-BrC6H4CNSC(Cl)N  
 Abstract    The title compound was obtained in 82% yield by the intramolecular cyclization of 4-BrC6H4C(NSCCl3)[N(SiMe3)2] in CH2CI2 at 23°C. It crystallizes in the triclinic system, space group PI, a = 7.957(3) Ä, b = 10.864(5) A, c = 5.625(1) A, a = 95.94(3)°, ß = 97.79(2)°, 7 = 100.72(3)°, V = 469.2(3) A3, and Z -2. The bond lengths of the planar C2N2S ring indicate partial 7r-delocalization. 
  Reference    Z. Naturforsch. 52b, 557—559 (1997); received September 5 1996 
  Published    1997 
  Keywords    Crystal Structure, 1, 2, 4-Thiadiazole, Intramolecular Cyclization 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0557.pdf 
 Identifier    ZNB-1997-52b-0557 
 Volume    52 
42Author    Tristram Chivers, Xiaorong Li, Masood ParvezRequires cookie*
 Title    Preparation and X-Ray Structure of 3,5-Dimethyl-1,4-dichloro-1,2,6- thiadiazine-1 -oxide  
 Abstract    The title compound was obtained by the reaction of 3,5-dimethyl-2//-l,2,6-thiadiazine-l,l-dioxide with PCI5 in chloroform. It crystallizes in the monoclinic system, space group P2\/c, a = 7.521(7) A, b = 8.400(4) A, c = 13.908(4) Ä, ß = 100.35(4)°, V = 864.4(8) A3, and Z = 4. The S(VI) atom lies 0.43 A out of the plane of the 7r-delocalized NCCCN unit. The mean S-N bond distance is 1.569(3) A. 
  Reference    Z. Naturforsch. 53b, 532—534 (1998); received December 18 1997 
  Published    1998 
  Keywords    Crystal Structure, 1, 2, 6-Thiadiazines, Sulfanuric Chloride 
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 TEI-XML for    default:Reihe_B/53/ZNB-1998-53b-0532.pdf 
 Identifier    ZNB-1998-53b-0532 
 Volume    53 
43Author    Bettina Eichhorn, Heinrich NöthRequires cookie*
 Title    New Diazasilaphosphetidines and their Precursors  
 Abstract    A series of aminosilanes (R 'H N bSiR : have been prepared. In case of bulky substituents R' the aminolysis of Ph^SiCb stops at the (R'HN)ClSiPh2 stage. Replacement of the Cl atom is achieved with LiNHR' which allows the synthesis o f mixed bisaminosilanes (R'HN)(R"HN)SiPh2. The X-ray structures of three of these compounds have been determined. There are no intermolecular N-H -N hydrogen bonds in these compounds in the solid state. Several 1,3,2,4-diazaphosphetidines have been synthesized using bis(N-lithioamino)silanes and bis(N-lithioamino)phosphanes . Amongst these the heterocycle 18 possesses an almost planar four membered N iSiP ring system. 
  Reference    Z. Naturforsch. 55b, 352—360 (2000); received January 18 2000 
  Published    2000 
  Keywords    Bis(monoorganylamino)diorganylsilanes, 1, 3, 2, 4-Diazasilaphosphetinides 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-0352.pdf 
 Identifier    ZNB-2000-55b-0352 
 Volume    55 
44Author    ProfG. Dr, MlostonRequires cookie*
 Title    Metallkomplexe  
 Abstract    mit funktionalisierten Schwefelliganden, XV [1]. Reaktionen von Platin(0)-Komplexen mit 1,2,4-Trithiolanen, 1,2,4,5-Tetrathianen, 1,2,3,5,6-Pentathiepanen sowie Thioketonen. Kristallstrukturanalyse von (Ph3P)2Pt(772-Ph2C=S) M etal Com plexes o f Functionalized Sulfur C ontaining Ligands, XV [1]. Reactions of Platinum(O) Com plexes w ith 1,2,4-Trithiolanes, 1,2,4,5-Tetrathianes, 1,2,3,5,6-Penta-thiepanes as well as Thioketones. X -R ay Structure A nalysis o f (Ph3P)2Pt(/72-Ph2C=S) W olfgang W eigand2, R alf W ünsch3, C hristian R obl3, Grzegorz M lostonb, Heinrich N öthc und M anfred Schm idt0 3,3,5,5-Tetraphenyl-1,2,4-trithiolane (1) reacts with twofold excess of (Ph3P)2Pt(?/2-C2H4) (4) to give a 1:1 mixture of the complexes (Ph3P)2Pt (SCPh2S) (6a) and (Ph3P)2Pt(?/2-Ph2C=S) (7a). Treatment of 3,3,6,6-tetraphenyl-l,2,4,5-tetrathiane (2) with a fourfold excess of 4 yields [Pt2(PPh3)4(/j-S)2] (8) and the platinum(O) compound 7a. The reaction of the 1,2,3,5,6-pentathiepane 3 with a fourfold excess of 4 affords a 1:1:1 mixture of 8, the platinum(O) complex 7b and the bis-thiolato platinum(II) complex 6b. The thioketone complexes 7a-c were formed in smooth reactions of 4 with the thioketones 5a-c. The molecular structure of (Ph3P)2Pt(?/2-Ph2C=S) (7a) has been established by single-crystal X-ray analysis. 
  Reference    Z. Naturforsch. 55b, 453—458 (2000); eingegangen am 28. Februar 2000 
  Published    2000 
  Keywords    1, 2, 4-Trithiolanes, Thioketones, Platinum Complexes 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-0453.pdf 
 Identifier    ZNB-2000-55b-0453 
 Volume    55 
45Author    Florian Breitsameter, Peter Mayer, Alfred SchmidpeterRequires cookie*
 Title    Die Kondensation von Ylidylchlorphosphanen mit Phosphanen und Bis(diphenylphosphanyl)methan und -amin The Condensation o f Ylidyl Chlorophosphines with Phosphines and Bis(diphenylphosphino)methane and -amine  
 Abstract    Ylidyl chlorophosphanes 1 and dichlorophosphanes 2 react with trimethylsilyl phosphanes to yield the ylidyl diphosphanes 3, 4,5, 7 and the 2-ylidyl triphosphanes 8. From the reaction of compounds 1 with lithium diphosphanyl amide and diphosphanyl methanide result the ylidyl diphosphonium ylides 11 and ylidyl diphosphinimines 13. The former rearrange to give the ylidyl triphosphanyl methanes 12. The chloromethyl diphosphinimine 13c enters a cyclization to give the 1,2,3,5-azatriphosphole derivative 14, the structure of which has been solved by X-ray analysis. From the reaction of ylidyl bis(chlorophosphanes) 17 and 20 with the same reagents the 1,2,4,5-tetraphosphinine derivative 18 and the 1,2,3,5,6-azatetraphosphinine derivatives 19 and 21 are obtained. 
  Reference    Z. Naturforsch. 55b, 519—526 (2000); eingegangen am 21. Februar 2000 
  Published    2000 
  Keywords    Phosphonium Ylides, Diphosphanes, 1, 2, 3, 5-Azatriphospholes 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-0519.pdf 
 Identifier    ZNB-2000-55b-0519 
 Volume    55 
46Author    Dorothee Petz, H. Ans-G, Erhard Löffler, Friedh SchneiderRequires cookie*
 Title    Inhibition of E. coli l -Asparaginase by Reaction with 2,3-Butanedione. Chemical Modification of Arginine and Histidine Residues  
 Abstract    The inactivation o f E. coli asparaginase by 2,3-butanedione studied with L-asparagine and dia-zooxonorvaline as substrates obeys pseudo first order kinetics. Activity losses are linear with re­ spect to arginine and histidine m odification, with com plete inactivation being correlated with alter­ ation o f one arginine and one histidine per subunit. The rate o f inactivation o f the enzym was re­ duced in the presence o f com petitive inhibitors like L-2-am ino-2-carboxyethane-sulfonam ide. U n ­ der comparable conditions 1,2-cyclo hexanedione does not affect the activity o f L-asparaginase. 
  Reference    Z. Naturforsch. 34c, 742 (1979); received May 8 1979 
  Published    1979 
  Keywords    Asparaginase, 2, 3-Butanedione, Arginine and Histidine Residues 
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 TEI-XML for    default:Reihe_C/34/ZNC-1979-34c-0742.pdf 
 Identifier    ZNC-1979-34c-0742 
 Volume    34 
47Author    Hamako Obata-Sasamoto, Atsushi Komamine, Koshi SaitoRequires cookie*
 Title    Biosynthesis of 3-Carboxy-6,7-dihydroxy-l, 2,3,4-tetra- hydroisoquinoline and l-Methyl-3-carboxy-6,7-dihydroxy-l, 2,3,4- tetrahydroisoquinoline in a Callus Culture of Stizolobium hassjoo  
 Abstract    dl-[/?-14C] 3,4-Dihydroxyphenylalanine (DOPA), [2-14C]pyruvate and [2-14C]acetate were ad­ ministered to a callus culture o f S. hassjoo and incorporation of the radioactivity into 3-carboxy-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline (I) and l-methyl-3-carboxy-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline (II) was examined. Incorporation of radioactivity from labelled DOPA into I and II, and from acetate into I were observed, while that from pyruvate into I and II and from acetate into II were hardly detected. The biosynthetic pathways o f I and D were discussed. 
  Reference    Z. Naturforsch. 36c, 921 (1981); received August 21 1981 
  Published    1981 
  Keywords    Stizolobium hassjoo, Biosynthesis, 3-Carboxy-6, 7-dihydroxy-1, 2, 3, 4-tetrahydroisoquinoline, 1 -Methyl-3-carboxy-6, 7-dihydroxy-1, 2, 3, 4-tetrahydroisoquinoline, Callus Culture 
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 TEI-XML for    default:Reihe_C/36/ZNC-1981-36c-0921.pdf 
 Identifier    ZNC-1981-36c-0921 
 Volume    36 
48Author    KenjiM. Atsui, H. Iroyuki, S. Hinta, T. Adahiko, K. Ajiwara, A. Kikazu, H. Atan AkRequires cookie*
 Title    Effect of Modification of Arginine Residues on the Activity of Soybean Lipoxygenase-1  
 Abstract    Arginine residues of soybean lipoxygenase-1 was modified with an arginine-directed chemical modifier, 2,3-butanedione. Although inactivation was not visible if the enzyme reac­ tion was monitored under the standard assay condition (83.3 |.im linoleic acid dispersed in 200 mM sodium borate, pH 9.0), rapid inactivation was observed with 5 mM sodium borate, pH 8.0. The inactivation was protected by the addition of a substrate, linoleic acid, in the modification mixture. Kinetic analyses indicated that one arginine residue accounted for the inactivation. Enzymological analyses showed that the modification narrowed the pH-activity profile of L-l and made L-l sensitive to salt concentration of the assay solution. Strong inactivation by modification was found at low salt concentration and low pH. This was not due to a physical change of the linoleic acid. On the other hand, product specificity of L-l was not altered after modification. Taken together, the modified arginine residue(s) was thought to be not essential to the catalysis but have an important role in supporting an ideal electrostatic interaction within L-l and/or between L-l and a substrate even in sub-optimal reaction conditions. 
  Reference    Z. Naturforsch. 50c, 37—4 (1995); received September 26/November 8 1994 
  Published    1995 
  Keywords    Arginine, 2, 3-Butanedione, Modification, Soybean Lipoxygenase-1 
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 TEI-XML for    default:Reihe_C/50/ZNC-1995-50c-0037.pdf 
 Identifier    ZNC-1995-50c-0037 
 Volume    50 
49Author    W. L. Driessen, P.L A EverstijnRequires cookie*
 Title    Metal(II) Complexes of 1,2,5-Oxadiazole  
 Abstract    A series of new coordination compounds is reported with 1,2,5-oxadiazole (ODZ) as the ligand, viz. [M(ODZ)3](SbCl 6)2 with M = Mg(II), Mn(U), Fe(II), Co(II), Ni(II), and Zn(II). The metal ions are in a regular octahedral environment of six nitrogen atoms. The ligands function as bidentate bridges between the metal ions. 
  Reference    Z. Naturforsch. 33b, 1120—1123 (1978); received June 12 1978 
  Published    1978 
  Keywords    Transition Metal Ions, 1, 2, 5-Oxadiazole, Ligand Field Spectra, IR 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-1120.pdf 
 Identifier    ZNB-1978-33b-1120 
 Volume    33 
50Author    Ger Vos, AnthonieJ. De Kok, GerritC. VerschoorRequires cookie*
 Title    Complexes of 1,2,4-Triazoles, Part XVII The Crystal Structure of Tris-/«-(4-ethyl-l,2,4-triazole-N l ,N 2 )- (4-ethyl-l,2,4-triazole-N 1 )-aquo-bis [bis(thiocyanato-N)- nickel(II)]hydrate, Ni2(C4N3H7)4(H20)(NCS)4 *H20 (x ~ 2.5)  
 Abstract    The crystal structure of Ni2(C4N3H7)4(H20)(NCS)4 • 2.5 H20 has been determined by X-ray diffraction techniques. The compound crystallizes in the monoclinic space group P2i/n with a — 15.121(4), 6= 13.237(2), c= 18.069(3), ß = 94.71(2)° and Z = 4; R = 0.040 (Rm = 0.051). The compound consists of dimeric units in which two Ni ions are bridged by three ethyltriazole (Ettrz) groups. For one Ni, two N donating NCS" groups and an Ettrz coordinating by only one N atom complete the NiNe octahedron. The other Ni atom, which is also octahedrally coordinated, has a coordinated water molecule instead of a monodentate Ettrz. 
  Reference    Z. Naturforsch. 36b, 809—813 (1981); received April 2 1981 
  Published    1981 
  Keywords    4-Ethyl-l, 2, 4-triazole, Binuclear Compound, Hydrogen Bonding 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-0809.pdf 
 Identifier    ZNB-1981-36b-0809 
 Volume    36 
51Author    Herbert Meier, Johannes Zountsas, Oswald ZimmerRequires cookie*
 Title      
 Abstract    A X H and 13 C NMR spectroscopical study is performed on the basis of 37 1,2,3-selena-diazoles. Besides the discussion of chemical shifts and coupling constants of X H and 13 C, selenium satellites were measured providing 1 H 77 Se and 13 C 77 Se coupling constants. 
  Reference    Z. Naturforsch. 36b, 1017—1022 (1981); eingegangen am 16. April 1981 
  Published    1981 
  Keywords    NMR Spectra, 1, 2, 3-Selenadiazoles, 77 Se Coupling 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-1017.pdf 
 Identifier    ZNB-1981-36b-1017 
 Volume    36 
52Author    Udo Plücken, Herbert MeierRequires cookie*
 Title    Lanthanide Induced Shifts in the »H and 13 C Nuclear Magnetic Resonance Spectroscopy for Structure Elucidations of Thiadiazole Oxides  
 Abstract    A systematic investigation of the LIS-method for structure elucidations is performed on the basis of thermally generated monoxides of 1,2,3-thiadiazoles. A calculation process for the evaluation of lanthanide induced shifts according to the McConnell-Robertson equa-tion was developed. The program can be applied to underdetermined systems with fewer variables than chemically not equivalent X H plus 13 C nuclei. A quality criterium for the method is given by 4-phenyl-l,2,3-thiadiazole-3-oxid -wellknown by an X-ray analysis. 
  Reference    Z. Naturforsch. 36b, 1305—1314 (1981); eingegangen am 21. Aprü 1981 
  Published    1981 
  Keywords    1, 2, 3-Thiadiazole-oxides, LIS Measurements, LIS Computer Program 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-1305.pdf 
 Identifier    ZNB-1981-36b-1305 
 Volume    36 
53Author    M. Torres, A. Clement, 0. P. StrauszRequires cookie*
 Title    Argon-Matrix Isolation of Bis(carbomethoxy)thiirene: Formation of Acyl and Carbalkoxythioketenes  
 Abstract    Photolysis of argon-matrix isolated 4,5-bis(carbomethoxy)-l,2,3-thiadiazole with A = 254 or 265 nm resulted in the almost quantitative formation of bis(carbomethoxy)-thiirene (3g). Photolysis of 3g could only be carried out by long irradiation times at short wavelength A = 210nm and resulted mainly in extensive fragmentation instead of the formation of bis(carbomethoxy)thioketene, confirming earlier predictions that substituents, especially electron-withdrawing ones, should stabilize the thiirene ring. Methylcarboethoxy and methylacetylthioketene were obtained, however, in the argon-matrix photolysis or flow thermolysis of 4-methyl-5-carboethoxy-or 4-carboethoxy-5-methyl-l,2,3-thiadiazole and 4-acetyl-5-methyl-l,2,3-thiadiazole, respectively. 
  Reference    Z. Naturforsch. 38b, 1208—1212 (1983); received June 6 1983 
  Published    1983 
  Keywords    Thiirene, Thioketene, 1, 2, 3-Thiadiazole, Thio-Wolff Rearrangement 
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 TEI-XML for    default:Reihe_B/38/ZNB-1983-38b-1208.pdf 
 Identifier    ZNB-1983-38b-1208 
 Volume    38 
54Author    Wim Vreugdenhil, MarcelF J Schoondergang, JaapG. Haasnoot, Jan ReedijkRequires cookie*
 Title    Magnetic and Spectroscopic Properties of Metal(II) Thiocyanate Compounds with 3,4-Dialkyl Substituted 1,2,4-TriazoIes  
 Abstract    Syntheses, spectroscopic and magnetic properties are described of a series of metal(II) thio-cyanate compounds with the asymmetric ligands 3-methyl-4-ethyl-l,2,4-triazole and 3-methyl-4-;-butyl-l,2,4-triazole. A dinuclear structure is proposed for the manganese, cobalt and nickel compounds based on the magnetic behaviour as well as on spectroscopic and analytical data. These compounds show antiferromagnetic interaction in the temperature range 4—80 K. The zinc compounds appear to be mononuclear, whereas a chain-like structure is proposed for the cad-mium compounds. 
  Reference    Z. Naturforsch. 42b, 791—795 (1987); received January 19 1987 
  Published    1987 
  Keywords    Asymmetric 1, 2, 4-Triazoles, Magnetic Exchange, Binuclear Compounds, Thiocyanate 
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 TEI-XML for    default:Reihe_B/42/ZNB-1987-42b-0791.pdf 
 Identifier    ZNB-1987-42b-0791 
 Volume    42 
55Author    Requires cookie*
 Title    Darstellung und Kristallstruktur von 2  
  Reference    (Z. Naturforsch. 47b, 1 [1992]) 
  Published    1992 
  Keywords    4, 6-Triferrocenyl-1, 3, 5, 2, 4, 6-triselenatriborinan 
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 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0001.pdf 
 Identifier    ZNB-1992-47b-0001 
 Volume    47 
56Author    MichaelW. Zenke, Karl HensenRequires cookie*
 Title    Phasendiagramme und Exzeßvolumina der Systeme (CH^SiCK/Pvridin und (CH3)2CC12/Pyridin  
 Abstract    The isobaric melting and boiling diagrams for the systems: dimethyldichlorosilane/pyridine and 2,2-dichloropropane/pyridine are reproduced. The existence of the incongruently melting addition compounds (CH3)2SiCl2 (Pyridine)2 and [(CH3)2CC12]3 • Pyridine could be proved. Some measurements of the molar volume of mixtures of pyridine and dimethyldichlorosilane, and pyridine and 2,2-dichloropropane are reported. For both systems the molar excess vol­ ume has been calculated as a function of the mole fractions. 
  Reference    Z. Naturforsch. 49b, 412—416 (1994); eingegangen am 20. September 1993 
  Published    1994 
  Keywords    Phase Diagrams, Pyridine, Dimethyldichlorosilane, 2, 2-Dichloropropane, Excess Volumes 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-0412.pdf 
 Identifier    ZNB-1994-49b-0412 
 Volume    49 
57Author    E. K. Yudin, K. V. Domasevitch, E. B. RusanovRequires cookie*
 Title    Crystal and Molecular Structure of Isonitrosomalonodiamido- (2,2-dipyridyl)copper(II), Chloride Monohydrate [Cu(Dipy){ONC(CONH2)2}Cl] H20  
 Abstract    The crystal and molecular structure of the complex [Cu(Dipy){NDA}Cl] • H 20 , where (NDA) = {ONC(CONH2)2}~ anion (space group P I, triclinic, with a = 7.834(1), b = 9.923(1), c = 9.952(1)A, a = 93.60(1), ß = 93.65(1), y = 92.72(1)°, Z = 2) has been determined from X-ray diffraction data. The structure was refined to R -0.029 for 2243 reflections with I>3ct(I). The coordination polyhedron of Cu2+ can be described as a distorted square pyra­ mid with a chlorine atom in the apex, and with the central atom situated 0.258(3) A above the base of the pyramid towards the chlorine atom. The complicated system of hydrogen bonding involving the water of crystallization connects copper complex units in to the chains in the c direction. 
  Reference    Z. Naturforsch. 50b, 864—866 (1995); received O ctober 17 1994 
  Published    1995 
  Keywords    Copper(II), Oximes, 2, 2-Dipyridyl, X-Ray Spectra 
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 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0864.pdf 
 Identifier    ZNB-1995-50b-0864 
 Volume    50 
58Author    Z. NaturforschRequires cookie*
 Title    Synthese und Dimerisierungsverhalten des l,l-Bis(trimethylsilyl)-2-(2,5-diisopropylphenyl)silens  
 Abstract    Tris(trim ethylsilyl)silylmagnesium bromide, (Me^SiX^SiMgBr, reacts with 2.5-diisopropyl-benzaldehyde to give 2,5-diisopropylphenyl-tris(trimethylsilyl)silylmethanol (1). With sodium 
  Reference    Z. Naturforsch. 51b, 370—3 (1996); eingegangen am 21. August 1995 
  Published    1996 
  Keywords    Silenes, Silene Dimerization, 2, 3-Disilanaphthalenes Tetrahydro, 1, 2-Disilacyclobutanes 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0370.pdf 
 Identifier    ZNB-1996-51b-0370 
 Volume    51 
59Author    JosephG. Robe, Duc Le Van, JostW. Innemöller, Bernt Krebs, M. Echtild LägeRequires 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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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0778.pdf 
 Identifier    ZNB-1996-51b-0778 
 Volume    51 
60Author    Clemens Krempner1, Rhett Kempeb, Hartmut Oehme3Requires cookie*
 Title    The Thermal Isomerization of a Tetrahydro-2,3-disilanaphthalene into a 1,2-Disilacyclobutane -The Conversion of a Formal Silene [2+4] Cyclodimer into the [2+2] Cycloadduct  
 Abstract    1,2,3,8a-Tetrahydro-1 -mesityl-5,7,8a-trimethyl-2,2,3,3-tetrakis(trimethylsilyl)-2,3-disila-naphthalene (3), the formal [2+4] cyclodimer of the transient 2-mesityl-l,l-bis(trimethylsilyl)-silene (2), on thermal treatment gradually isomerizes to give a mixture of the [2+2] products (E)-and -predominantly -(Z)-3,4-dimesityl-1,1,2,2-tetrakis(trimethylsilyl)-l,2-disilacyclo-butane [(E/Z)-4], By prolonged heating or at higher temperatures both (E/Z)-3 and (Z)-4 are converted into (E)-4, the thermodynamically most stable head-to-head dimer of 2. Possible pathways of the isomerization processes are discussed. 
  Reference    Z. Naturforsch. 52b, 815—818 (1997); received February 14 1997 
  Published    1997 
  Keywords    Silenes, Silene Dimerization, 2, 3-Disilanaphthalene Tetrahydro, 1, 2-Disilacyclobutane 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0815.pdf 
 Identifier    ZNB-1997-52b-0815 
 Volume    52 
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