| 5 | Author
| M. Bruns, W. Preetz | Requires cookie* | | Title
| Darstellung  | | | Abstract
| , spektroskopische und elektrochemische Charakterisierung von Pentachloromonocarbonylosmat(IY), [OsCl5(C O)]_ Preparation, Spectroscopical and Electrochemical Characterization of Pentachlorom onocarbonylosm ate(IV), [OsCl5(CO)]~ | | |
Reference
| (Z. Naturforsch. 41b, 25 [1986]) | | |
Published
| 1986 | | |
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| default:Reihe_B/41/ZNB-1986-41b-0025.pdf | | | Identifier
| ZNB-1986-41b-0025 | | | Volume
| 41 | |
6 | Author
| | Requires cookie* | | Title
|  | | | Abstract
| Die vorliegende Arbeit beschreibt Synthese und Struktur von 1,2,3-Azadiboriridinen 7 [8]. Synthese | | |
Reference
| (Z. Naturforsch. 41b, 32 [1986]) | | |
Published
| 1986 | | |
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| default:Reihe_B/41/ZNB-1986-41b-0032.pdf | | | Identifier
| ZNB-1986-41b-0032 | | | Volume
| 41 | |
7 | Author
| Guido Wenski, A. Lbrecht Mewis | Requires cookie* | | Title
| B aA l4-Strukturvarianten bei  | | | Abstract
| A R u2X 2 (A = Ca, Sr, Ba, Eu; X — P, As) und A P t2P2—x i A = Ca, Eu) BaA l4-D envative Structures of / I R u ^ (A = Ca, Sr, Ba. E u; X = P. As) and of /lP t2P2_,. Ternary Interm etallic Pnictides, 2 A E lem ents, Europium , Crystal Structure Com pounds /1R u 2P (A s) 2 (A = Ca, Sr, Ba, E u) were found to have the ThCr2Si2-type structure | | |
Reference
| (Z. Naturforsch. 41b, 38—43 [1986]; eingegangen am 3. O ktober 1985) | | |
Published
| 1986 | | |
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| default:Reihe_B/41/ZNB-1986-41b-0038.pdf | | | Identifier
| ZNB-1986-41b-0038 | | | Volume
| 41 | |
8 | Author
| H. Küppers, H.-HE. Ulert, K.-F Hesse, W. Kalz, H. Hom | Requires cookie* | | Title
| Synthesis and Crystal Structure of Di[bis(triphenylphosphine)iminium]-biscyanophthalocyaninato-ferrate(II)- dichloromethane  | | | Abstract
| Phthalocyanine-cyano-iron(II), Preparation, Crystal Structure Black-green crystals o f [[(C6H 5)3P]2N ]2[F e(C N)2(C 32H 16N 8)] • C H 2C12 (triclinic, P I ; a = 14.306, b = 13.205, c = 12.081 Ä ; a = 98.77, ß = 92.15, y = 92.60°; Z -1) are prepared by the reaction of [[(C6H 5) 3P ]2N]C N and chlorophthalocyaninato-iron(III) in basic media. The crystal structure was refined to Rw — 4.6% for 3617 reflections measured at 180 K. The Fe(II) ion is coordinated by six nearly equidistant ligands that form an almost regular octahedron suggesting low-spin configuration. | | |
Reference
| (Z. Naturforsch. 41b, 44 [1986]; received O ctober 1. 1985) | | |
Published
| 1986 | | |
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| default:Reihe_B/41/ZNB-1986-41b-0044.pdf | | | Identifier
| ZNB-1986-41b-0044 | | | Volume
| 41 | |
9 | Author
| Elke Conradi, H. Eribert, W. Adle, Ulrich Müller, Kurt Dehnicke | Requires cookie* | | Title
| AsPh4[W (0)Cl3(HN3S2)]; Synthese, IR-Spektrum und Kristallstruktur  | | | Abstract
| O xo-trichloro-hydrocyclothiazeno-tungstate(V I), Synthesis, IR Spectrum, Crystal Structure V iolet crystals o f A sPh4[W (0)C l3(H N 3S2)] were obtained by partial hydrolysis o f A sP h4 [W Cl4(N 3S2)] in a saturated solution in C H 2C12/CC14. Its IR spectrum is reported. The crystal structure was determ ined by X-ray diffraction (2284 independent observed reflexions, R = 0.041). Crystal data: triclinic, space group P 1, Z = 2, a = 812.2, b = 1268.4, c = 1343.9 pm , a = 88.58, ß = 82.04 and y = 88.26°. The com pound consists o f A sPh4® cations and [W (0)C l3(H N 3S2) ]e anions in which the tungsten atoms have a distorted octahedral coordination with one oxo-ligand (171 pm), three chlorine atoms and two nitrogen atoms o f the planar (H N 3S 2) 2 0 ligand. The WN bond lengths are 183 and 226 pm; the longer WN bond is due to the hydrogen atom attached to its N atom and to the trans influence o f the oxo group. The crystal packing corresponds to one o f the types frequently found among tetraphenylphosphonium com pounds with cations stacked to parallel columns. | | |
Reference
| (Z. Naturforsch. 41b, 48 [1986]; eingegangen am 7. O ktober 1985) | | |
Published
| 1986 | | |
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| default:Reihe_B/41/ZNB-1986-41b-0048.pdf | | | Identifier
| ZNB-1986-41b-0048 | | | Volume
| 41 | |
10 | Author
| H. Erbert, W. Roesky, Jörg Sunderm, M. Athias, N. Oltemeyer, GeorgeM. Sheldrick, Karen Meyer-Bäse, PeterG. Jones | Requires cookie* | | Title
| Darstellung und Struktur des N-Thiobis-N' -(phenylsulfonyl)schwefeldiimids Synthesis and Structure of N-Thiobis-N'-(phenylsulfonyl)sulfurdiimide  | | | Abstract
| The reaction of S4N 4 with P h S 0 2N C l2 proceeds with formation o f (P h S 0 2N S N)2S 2. The main product 2 was characterized by an X-ray structure determination. [P2]/c, a = 996.8(2), b = 1733.0(2), c = 1131.2(1) pm, ß = 114.69(1)°, Z = 4, R — 0.044 for 1911 reflections.] 2 contains a | | |
Reference
| (Z. Naturforsch. 41b, 53—58 [1986]; eingegangen am 27. Septem ber 1985) | | |
Published
| 1986 | | |
Keywords
| Sulfur Nitrogen C om pound, Crystal Structure, cis-trans Configuration, Metal Com plex | | |
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| default:Reihe_B/41/ZNB-1986-41b-0053.pdf | | | Identifier
| ZNB-1986-41b-0053 | | | Volume
| 41 | |
11 | Author
| BerndW. Rackmeyer | Requires cookie* | | Title
| Methylaminodiphenylborane — Application of n B, 13C, 14N, 15N NMR  | | | Abstract
| BC(pp)?r Interactions, N M R Spectra, R otation about the B N bond UB , 13C , 14N , 15N N M R is used to study m ethylam inodiphenylborane (1). Com pound 1 can be regarded as a m odel com pound for studying BN(pp)jr-, B C (p p)7r interactions, for determining the barrier to rotation about the B —N bond and for the application o f natural abundance 15N N M R to boron-nitrogen chemistry. The 13C N M R o f 1 shows a large splitting o f the uC (para) resonances (in contrast to reports on similar com pounds in the literature) as a consequence o f hindered rotation about the BN bond. The difference in the nC (para) nuclear shielding indicates different m esom eric interactions between the trigonal boron atom and the two phenyl groups. | | |
Reference
| (Z. Naturforsch. 41b, 59 [1986]; received July 23/Septem ber 13 1985) | | |
Published
| 1986 | | |
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| default:Reihe_B/41/ZNB-1986-41b-0059.pdf | | | Identifier
| ZNB-1986-41b-0059 | | | Volume
| 41 | |
12 | Author
| Ekkehard Fluckb, Jürgen Svara2 | Requires cookie* | | Title
| NMR-Untersuchungen an 3,3-Difluor-2-ethyI-l,l>2-tris(diethoxyphosphoryI)-cyclopropan  | | | Abstract
| Investigation of 3,3-D ifluoro-2-ethyl-l,l,2-tris(diethoxyphosphoryl)cyclopropane G ernot H eckm ann3, 3 ,3-D iflu oro-2-eth yl-l. 1,2-tris(diethoxyphosphoryl)cyclopropane. NM R Spectra. Triple Resonance The 19F , 31P and 13C NM R spectra in double and triple resonance m ode and the tem perature dependence o f the N M R parameters o f the title compound are discussed in detail. The rotational behavior o f the phosphoryl groups is described; two o f these groups show equal barriers to rotation o f 75 kJ m ol-1, the third one is rotating freely at room temperature. | | |
Reference
| (Z. Naturforsch. 41b, 63—69 [1986]; eingegangen am 30. Septem ber 1985) | | |
Published
| 1986 | | |
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| default:Reihe_B/41/ZNB-1986-41b-0063.pdf | | | Identifier
| ZNB-1986-41b-0063 | | | Volume
| 41 | |
13 | Author
| Lutz Dahlenburg, Bernd Pietsch | Requires cookie* | | Title
| Oligophosphan-Liganden, X I V [1 ]  | | | Abstract
| Bis(distickstoff)molybdän-Komplexe M o(N 2)2[PhP(CH 2CH 2CH 2PPh2)2](PR3) Oligophosphine Ligands, XIV [1] Bis(dinitrogen)m olybdenum Complexes M o(N2)2[PhP(CH2CH 2C H2PPh2)2](P R 3) D initrogen. Bis(3-diphenylphosphinopropvl)phenylphosphine. M olybdenum C om plexes. • "P N M R Spectra. X -R ay. D eterm ination | | |
Reference
| (Z. Naturforsch. 41b, 70—75 [1986]; eingegangen am 19. Juni/27. September 1985) | | |
Published
| 1986 | | |
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| default:Reihe_B/41/ZNB-1986-41b-0070.pdf | | | Identifier
| ZNB-1986-41b-0070 | | | Volume
| 41 | |
15 | Author
| M. =. Cr, Mo, W. Preparation, N.M R Spectroscopy, Paul Peringer | Requires cookie* | | Title
| Darstellung und NMR-Spektroskopie der Argentat-Komplexe [Ag{(ji-PR2)M(CO)5}2]  | | | Abstract
| of the Argentate Complexes [Ag{(w-PR2)M (C O)5}2] , M = Cr, Mo, W D agm ar O bendorf A rgentate. Phosphido. Pentacarbonylm etal. NM R Spectra The products o f the reaction betw een [A gC l(dppe)], [M (C O)5P R 2H ] and TIOEt are the ionic com plexes [A g (7/ 2-d p pe)2L [A g {(a -P R 2)M (C O)5}2L , R = Ph, M = Cr, M o, W; R = Cy, M = Cr (dppe = (C H 2P Ph2)2, Cy = C yclohexyl). The silver(I)-phosphido-ate title com plexes are also accessible from A g Ö 3SC F3, [M (C O)5P R 2H] and Et2N H or M eO ~. Asym m etric phosphido argen-tates o f the type [A g{(w -PR 2)M (C O)5}{(w -PR 2)M '(CC))5 }]_ , R = R' = Ph; M , M' = Cr, M o, W; M ^ M '. R = Ph, R' = Cy, M = Cr, M o, W , M' = Cr are formed via synproportionation of the respective sym metric com pounds. The new com plexes were characterized by 31P N M R spectroscopy. | | |
Reference
| (Z. Naturforsch. 41b, 79 [1986]; eingegangen am 23. Septem ber 1985) | | |
Published
| 1986 | | |
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| default:Reihe_B/41/ZNB-1986-41b-0079.pdf | | | Identifier
| ZNB-1986-41b-0079 | | | Volume
| 41 | |
16 | Author
| M. L. Dhar, O.Nkar Singh | Requires cookie* | | Title
| Nature and Composition of Fe(III) Complexes with Some Polyphenolic Ligands  | | | Abstract
| Chelates Com plexes o f F e(III), Polyphenolic Ligands The chelated com plexes of Fe(III) of the type FeL3 [where L is the m ononegative anion of phloroacetophenone (P H A); 2 ,4 -dim ethoxyphloroacetophenone (D M P H A); 4-benzyloxyres-acetophenone (B R P); 2,6-dihydroxyphenylbenzylketone (D H P B K); 2,4,6-trihydroxyphenyl-4'-m ethoxybenzylketone (T H P B K); 2-hydroxy-4,6-dibenzyloxyphenyl-3',4'-dioxym ethylenebenzyl-ketone (H B M K); 2-hydroxy-3-prenyl-4' ,6'-dibenzyloxyphenyl-3' ,4'-dioxym ethylenebenzyl-ketone (H PBM K); naringenin (N G); 2 -m ethyl-5 ,7 -dihydroxychrom one (M D H C) and methyl-/?-resorcylate (M R)] have been prepared and characterized by elem en tal, m agnetic, infrared and electronic spectral studies. | | |
Reference
| (Z. Naturforsch. 41b, 82—8 [1986]; received August 2. 1985) | | |
Published
| 1986 | | |
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| default:Reihe_B/41/ZNB-1986-41b-0082.pdf | | | Identifier
| ZNB-1986-41b-0082 | | | Volume
| 41 | |
17 | Author
| RichardM. Ynott, W. Olf, Jürgen Richter, G.Ünther Wilke | Requires cookie* | | Title
| Determination of the Enantiomeric Excess of Horner Phosphines by 13C NMR Spectroscopy. A 13C and 31P NMR Study of the Diastereomeric Complexes Formed with [i/3-(+)(lR ,5R )-Pinenyl]nickel Bromide Dimer  | | | Abstract
| ohlenforschung, K aiser-W ilhelm -Platz 1, D-4330 M ülheim a. d. Ruhr, Federal Republic o f G erm any The 13C and 31P N M R data o f the H orner phosphines PRR'R" [R — M e. R' = f-Bu. R" = Ph (2) or /-Pr (4)] and their diastereom eric 1:1 adducts with [?73-(+) (l R .5R)-pinenyl]nickel bromide dimer (3) and (5), respectively, are reported. It is shown that the optical purities of the phosphines can be deduced easily from the N M R spectra. N ot only are these values in very good agreem ent with those obtained from optical rotatory data but they are also obtained much more con ve niently. | | |
Reference
| (Z. Naturforsch. 41b, 85 [1986]; received A ugust 141985) | | |
Published
| 1986 | | |
Keywords
| Horner Phosphines, D eterm ination o f Optical Purity, 3IP NM R Spectra, 13C NM R Spectra | | |
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| default:Reihe_B/41/ZNB-1986-41b-0085.pdf | | | Identifier
| ZNB-1986-41b-0085 | | | Volume
| 41 | |
19 | Author
| Richard Neidlein, G. Ernot, G. Ünther, W. Alter Kramer, Alfred Gieren, Viktor Lamm, H. Elm, Ut Betz | Requires cookie* | | Title
|  | | | Abstract
| Synthesis, D ouble Coupling R eaction, l,6-M ethano[10]annulenyl-bis-arylhydrazone, X -R ay, Bonding Relationships The synthesis o f 8a by coupling reaction o f 2.10-dim ethoxy-l,6-m ethano[10]annulene (6) with 2-nitro-4-chlorophenyl-diazonium -tetrafluoroborate (7) as well as its spectroscopic properties are described; an X-ray structure analysis o f 8 a x CHC13 is reported. | | |
Reference
| (Z. Naturforsch. 41b, 93 [1986]; eingegangen am 19. August 1985) | | |
Published
| 1986 | | |
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| default:Reihe_B/41/ZNB-1986-41b-0093.pdf | | | Identifier
| ZNB-1986-41b-0093 | | | Volume
| 41 | |
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