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1Author    Birgit Lehnis, Joachim SträhleRequires cookie*
 Title    Synthese und Kristallstruktur von C83(AuBr 4 ) 2 Br3 Synthesis and Crystal Structure of Cs3(AuBr4) 2 Br 3  
 Abstract    Cs3(AuBr4)2Br3 is obtained in the form of red needles by adding the stoichiometric amount of CsBr to a solution of HAuBr4 and Br3~ in aqueous HBr. The salt decomposes slowly at room temperature to form a mixed-valent, cubic bromo aurate(I,III), in which the linear AuBr 2 ~ ions are partially substituted by Br3~ ions. At 140 °C Cs 2 Au 2 Bre and CsBr are formed. Cs3(AuBr4) 2 Br3 crystallizes monoclinic with four formula units in the space group P2i/c. The structure is built up by AuBr 4 ~ and Br3~ anions and Cs+ cations. An average Au-Br distance of 242.2 pm was found for the square planar AuBr 4 ~ ion. The linear Br3~ groups are almost symmetrical with Br-Br distances of 254.0 and 256.2 pm. Therefore only two vibrations are observed in the IR spectrum: Vas = 172, <5 = 56 cm -1 . The absorptions of the AuBr 4 _ groups are: vas = 250, <5as= 113, y — 102 cm -1 . 
  Reference    Z. Naturforsch. 36b, 1504—1508 (1981); eingegangen am 8. September 1981 
  Published    1981 
  Keywords    Synthesis, IR Spectra, Crystal Structure 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-1504.pdf 
 Identifier    ZNB-1981-36b-1504 
 Volume    36 
2Author    Hans Zimmer, Madhusudan Jayawant, Adel Amer, BruceS. AultRequires cookie*
 Title    Reactions of Alkylamino-and Dialkylaminotriphenylphosphonium Halides with Halogens and Interhalogen Compounds; Formation of Alkylaminotriphenylphosphonium Polyhalides  
 Abstract    Alkylamino-and cycloalkylaminotriphenylphosphonium halides react with elemental halogens or interhalogen compounds to afford alkylamino-or cycloalkylaminotriphenyl-phosphonium trihalides. The stability of these trihalides depends on the cation as well as the trihalide anion. The assignment of a trihalide structure to these compounds was based on elemental analysis and on IR-and Raman spectroscopic evidence. Most stable are the tribromide and [1X2]° salts. During all reactions involving N-alkylamino-and N-cyclo-alkylaminotriphenylphosphonium halides and elemental halogens an N-halogenation of the cation was not observed. 
  Reference    (Z. Naturforsch. 38b, 103—107 [1983]; received September 20 1982) 
  Published    1983 
  Keywords    Halides, IR Spectra, Raman Spectra 
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 TEI-XML for    default:Reihe_B/38/ZNB-1983-38b-0103.pdf 
 Identifier    ZNB-1983-38b-0103 
 Volume    38 
3Author    M. Bobadilla, M. MoránRequires cookie*
 Title    Oxidative Addition of Pseudohalogen to [P(OPh)3]4Ni  
 Abstract    The title compound reacts with cyanogen halides, XCN (X = Br or I) to give the com-plexes L2(X)(CN)Ni (L = P(OPh)3, X = Br or I). The oxidative addition of (SCN)2 and (SeCN)2 to the same compound results in the formation of L2Ni(XCN)2 (X = S or Se). All the complexes have been characterized by elemental analysis, and IR, iH NMR and electronic spectra. 
  Reference    Z. Naturforsch. 38b, 1069—1071 (1983); received May 13 1983 
  Published    1983 
  Keywords    Pseudohalogens, IR Spectra, Nickel 
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 TEI-XML for    default:Reihe_B/38/ZNB-1983-38b-1069.pdf 
 Identifier    ZNB-1983-38b-1069 
 Volume    38 
4Author    M-S Delgado, M-J Macazaga, J.R M AsaguerRequires cookie*
 Title    Oxidative Addition Reactions of P(CN)" P(NCO)3 and P(NCS), to (i/5-C5Me5 )Co(CO)2  
 Abstract    The phosphorus pseudohalogens P(CN)3, P(NCO)3 and P(NCS)3 react with (?/5-C5Me5)C o(C O)2 to give the complexes (?75-C;Me5)Co(CO)XPX2 (X = CN, NCO, NCS). All the compounds are characterized by elemental analysis, IR. electronic and 'H NMR spectra. 
  Reference    Z. Naturforsch. 39b, 142 (1984); received October 3 1983 
  Published    1984 
  Keywords    Phosphorus Pseudohalogens, IR spectra, Cobalt 
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 TEI-XML for    default:Reihe_B/39/ZNB-1984-39b-0142.pdf 
 Identifier    ZNB-1984-39b-0142 
 Volume    39 
5Author    Gerhard Beber, Jürgen Hanich, Kurt DehnickeRequires cookie*
 Title    Reaktionen von Yanadiumtetrachlorid mit Trithiazylchlorid Reactions of Vanadium Tetrachloride with Trithiazylchloride Vanadiumtrichloride-Thiazylchoride Adduct, Tetrachlorovanadate(III)-S 2 N 2  
  Reference    (Z. Naturforsch. 40b, 9—12 [1985]; eingegangen am 24. September 1984) 
  Published    1985 
  Keywords    Adduct, Preparation, IR Spectra 
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 TEI-XML for    default:Reihe_B/40/ZNB-1985-40b-0009.pdf 
 Identifier    ZNB-1985-40b-0009 
 Volume    40 
6Author    Bernhard Czeska, Kurt DehnickeRequires cookie*
 Title    [P(C 6 H 5 ) 4 ] 2 S 8 : Synthesis and IR Spectrum  
 Abstract    [P(C 6 H 5)4] 2 S g was prepared from Na 2 S 4 and PPh 4 Cl in ethanol solution and characterized by its IR spectrum. 
  Reference    (Z. Naturforsch. 40b, 120—121 [1985]; eingegangen am 28. September 1984) 
  Published    1985 
  Keywords    Tetraphenylphosphonium Octasulfide, Synthesis, IR Spectra 
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 TEI-XML for    default:Reihe_B/40/ZNB-1985-40b-0120_n.pdf 
 Identifier    ZNB-1985-40b-0120_n 
 Volume    40 
7Author    H. Eribert, W. Adle, Kurt Dehnicke, D. Ieter FenskeRequires cookie*
 Title    (AsPh4)4[CrCl4(/J-N2S2)]4 * 8 CH2C12; Synthese, IR-Spektrum und Kristallstruktur (A sPh4)4[CrCl4(w-N2S2)]4 -8 CH 2C12; Synthesis, IR Spectrum and Crystal Structure  
 Abstract    Trithiazylchloride, (NSC1)3, reacts with metallic chrom ium, with chromium hexacarbonyl, with CrCl3-3 thf, as well as with chrom ium (VI) oxide to form mixtures, in which S4N 3®[CrCl4(N 2S2) ] 0 can be identified as the major product. This com pound reacts with tetraphenylarsonium chloride in dichlorom ethane to form the title com pound, which we have characterized by IR spectroscopy and an X-ray crystal structural analysis. (A sP h4)4[CrCl4(N 2S2)]4 -8 C H 2C12 crystallizes m onoclini-cally in the space group C 2 /c with four formula units per unit cell and with the follow ing lattice constants at —100 °C: a = 2146, b = 2033, c = 3137 pm; ß = 96.0° (9918 independent observed reflexions, R = 0.064). The com pound consists o f A sPh4® ions, tetrameric anions [CrCl4(N 2S2)]44e and included C H 2C12 m olecules. The chromium atom s of the anions occupy the corners o f a nearly ideal square; they are connected via the N -atom s o f planar N 2S2-rings, which are oriented perpendicularly to the Cr4-plane. The chromium atom s com plete their distorted octahedral coordination with four terminal chlorine atom s, the axial ones o f which form short Cl---S-contacts o f average 310 pm to the S-atom s o f the N 2S2-rings. 
  Reference    Z. Naturforsch. 40b, 1314—1319 (1985); eingegangen am 2. Mai 1985 
  Published    1985 
  Keywords    Trithiazylchloride, IR Spectra, Crystal Structure 
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 TEI-XML for    default:Reihe_B/40/ZNB-1985-40b-1314.pdf 
 Identifier    ZNB-1985-40b-1314 
 Volume    40 
8Author    J. Fritze, W. PreetzRequires cookie*
 Title    c/osö-Halogenohydrohexaborate, III Schwingungsspektren der c/oso-Halogenohydrohexaborate X"B  
 Abstract    ~, n = 1-5; X = Cl, Br, I c/oso-Halogenohydrohexaborate, III Vibrational Spectra of the c/oso-Halogenohydrohexaborates X"B 6 H 6 _" 2_ , n = 1-5; X = Cl, Br, I The IR and Raman spectra of 20 different halogenohydrohexaborates, including pairs of geometric isomers of the series X"B 6 H 6 _ n :_ , X = Cl, Br, I; n = 1—5, have been assigned according to their point groups D 4h , C 4v , C 3v and C 2v determined previously by NMR studies. Due to weak coupling, the vibrations are treated separately to a first approximation in terms of internal B 6 -cage modes on one hand and modes of the substituents against the cage entity on the other hand. Disregarding the splitting by lowered symmetry, depending on the degree of halogenation, all internal modes of the B 6 cluster are observed at nearly unchanged positions in the range of 450—1250 cm -1 . The B 6 —X stretching vibrations, however, exhibit significant shifts to lower energy with increasing mass of substituents. 
  Reference    Z. Naturforsch. 42b, 293—300 (1987); eingegangen am 21. November 1986 
  Published    1987 
  Keywords    Halogenohydrohexaborates, IR Spectra, Raman Spectra 
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 TEI-XML for    default:Reihe_B/42/ZNB-1987-42b-0293.pdf 
 Identifier    ZNB-1987-42b-0293 
 Volume    42 
9Author    N.K D, A.K S En, G.Requires cookie*
 Title    Chemistry of Lanthanons, XLII Preparation and Characterization of Isonicotine and Picoline Hydrazide Complexes of Lanthanons  
 Abstract    Rare 
  Reference    (Z. Naturforsch. 30b, 769—772 [1975]; received May 5/June 16 1975) 
  Published    1975 
  Keywords    Earth Complexes, Conductance, Thermal Analysis, IR Spectra 
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 TEI-XML for    default:Reihe_B/30/ZNB-1975-30b-0769.pdf 
 Identifier    ZNB-1975-30b-0769 
 Volume    30 
10Author    Requires cookie*
 Title    Komplexchemie polyfunktioneller Liganden  
 Abstract    , XXXV1 Das Reaktionsverhalten von Co2(CO)8 gegenüber dem tritertiären Phosphin l.l.l-Tris(diphenylphosphinomethyl)äthan Complex Chemistry of Polyfunctional Ligands, X X X V 1 Reaction o f Co2(CO)8 w ith the T ritertiary Phosphine 1,1,1-Tris(diphenylphosphinom ethyl)ethane J o c h e n E l l e r m a n n und J o a c h i m F. S c h i n d l e r Octacarbonyldicobalt reacts with the tritertiary phosphine l,l,l-tris(diphenylphosphino-methyl)ethane (TDPME) to give the ionic complex [Co(CO)2TDPME][Co(CO)4]. Treat­ ment of [Co(CO)2TDPME][Co(CO)4] with Na[B(CeH5)4], HCIO4 and CH3J yields the 
  Reference    (Z. Naturforsch. 30b, 914—919 [1975]; eingegangen am 7. Juli 1975) 
  Published    1975 
  Keywords    Cobaltcarbonyl Derivatives, Tritertiary Phosphine, Raman Spectra, IR Spectra 
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 TEI-XML for    default:Reihe_B/30/ZNB-1975-30b-0914.pdf 
 Identifier    ZNB-1975-30b-0914 
 Volume    30 
11Author    Heinrich Homborg, Wilhelm Preetz, Günes Barka, Gernot SchätzelRequires cookie*
 Title    Darstellung und spektroskopische Charakterisierung von Tetrahalogenooxalato-Osmaten(IY)  
 Abstract    Reaction of [OsXe] 2-(X = CI, Br, I) with oxalic acid in water gives the very stable and deeply coloured new complexes [OsX40x] 2-which can be precipitated as alkali or tetra-alkylammonium salts. The salts with long-chain alkylammonium ions are soluble in all common no polar solvents. The IR and Ra spectra and the depolarization ratios are consistent with the local C2v-symmetry. The coupling between the vibrations of co-ordinated oxalate and with the skeletal [OsX402]-modes is apparently small. The optical spectra have been studied at low temperature (10 K). Analogous to [OsXe] 2-the very intense absorptions in the UV and VIS are assigned to the electric dipole allowed electron transfer from "(jr+cr)tiu, 7rt2U(y7), 7it2u(y8) and (<r-f-7r)tiu" to "dt2g". By the descent in symmetry each of these transitions is further split in three components (Ai, Bi, B2) corresponding to the three different groups of ligands, X2 tr -, X2 C -and ox. The distinction between the X2 tr --*-Os and X2 C --> Os is caused by a static trans-effect and depends on the difference of the optical electronegativities induced by ox. This splitting is not observed for [OsCLiox] 2 -but is about 900 cm-* for [OsBr4ox] 2 -and 1200 cm" 1 for [OsI4ox] 2 -. The well defined bands in the NIR and VIS are assigned to the intraconfigurational d-d-transitions between the spin-orbit components in the octahedral doublegroup Oh* splitted by the lower C2v-symmetry. Some of the zero-phonon transitions within the split of the 3 Tig, Oh-groundstate exhibit extremely high intensities (e~2500 cm 2 /mmol). The assign-ment of these transitions is improved by the electronic Ra spectra. The finestructure of some of the d-d-transitions originates from coupling with Ai vibrational modes especially with Vs(C-O). 
  Reference    Z. Naturforsch. 35b, 554—563 (1980); eingegangen am 10. Dezember 1979 
  Published    1980 
  Keywords    Tetrahalooxalato-osmates(IV) UV-VIS Spectra, IR Spectra, Raman Spectra 
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 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0554.pdf 
 Identifier    ZNB-1980-35b-0554 
 Volume    35 
12Author    Kurt Dehnicke, Rainer LößbergRequires cookie*
 Title    Preparation and IR Spectrum of 0s04 * 2 SbCl5  
 Abstract    Osmiumtetroxide and antimony pentachloride form a donor acceptor complex, 0s04 • 2 SbCls. According to the IR spectrum the complex contains OsOSb bridges. With VCLj, TiCU, M0CI5 and osmiumtetroxide rapid ligand exchange reactions occur, forming VOCI3, TiOCl2 and several oxochlorides of molybdenum and OsCLi, respectively. 
  Reference    Z. Naturforsch. 35b, 1587—1588 (1980); eingegangen am 4. August 1980 
  Published    1980 
  Keywords    Preparation, IR Spectra, Osmiumtetroxide-Antimonypentachloride Donor-Acceptor Complex 
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 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-1587_n.pdf 
 Identifier    ZNB-1980-35b-1587_n 
 Volume    35 
13Author    Emmanuel Chukwuemeka OkaforRequires cookie*
 Title    The Metal Complexes of Heterocyclic /?-Diketones and their Derivatives, Part VIII Synthesis, Structure, Proton NMR and Infrared Spectral Studies of the Complexes-Phenyl-3-methyl-4-trifluoroacetyl-pyrazolone-5 (HPMTFP)  
 Abstract    of Al(in), Fe(ffl), Co(ffl), Rh(m), In(ffl), and Zr(IV) with l New complexes of Al(III), Fe(III), Co(III), Rh(III), In(III) and Zr(IV) with 1-phenyl-3-methyl-4-trifluoroacetyl-pyrazolone-5, (HPMTFP), have been synthesized and charac-terized by means of elemental analyses, conductivity and magnetic moment measurements, proton NMR and infrared spectroscopy. It is concluded that the ligand, HPMTFP, reacts as a bidentate enol forming neutral metal chelates. The PMR spectra of chelates suffi-ciently soluble in deuterated NMR solvents were recorded and studied. The IR spectra are measured between 4000-200 cm -1 and assignments are proposed for the observed fre-quencies. The M-0 stretching frequency follows the order: AI > Rh > Fe — Co = Zr > In. 
  Reference    Z. Naturforsch. 36b, 213—217 (1981); received September 17 1980 
  Published    1981 
  Keywords    Metal Complexes, PMR Spectra, IR Spectra 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-0213.pdf 
 Identifier    ZNB-1981-36b-0213 
 Volume    36 
14Author    Römer, H. Scholl, H. Budzikiewicz, H. Korth, G. PulvererRequires cookie*
 Title     
 Abstract    The structure elucidation of several minor phenazine pigments of Pseudomonads is described. 4-Hydroxyphenazine-l,6-dicarboxylic acid dimethyl ester, 2,3-dihydroxy-phenazine, 2,3,7-trihydroxyphenazine, 4-hydroxyphenazine-l-carboxylic acid, 2,3-di-hydroxyphenazine-l-carboxylic acid, 2,6-dihydroxyphenazine-l-carboxylic acid and 2,3,7-trihydroxyphenazine-l,6-dicarboxylic acid are new phenazine derivatives. The distribu-tion of phenazines in the genus Pseudomonas is investigated. 
  Reference    Z. Naturforsch. 36b, 1037—1046 (1981); eingegangen am 27. März 1981 
  Published    1981 
  Keywords    Phenazines, Bacterial Constituents, Pseudomonads, NMR Spectra, IR Spectra 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-1037.pdf 
 Identifier    ZNB-1981-36b-1037 
 Volume    36 
15Author    S. P. Perlepes, ThF. Zafiropoulos, A. K. Anagnostopoulos, A. G. GalinosRequires cookie*
 Title    Compounds of Complex Halo and Pseudohalo Acids of the Group IIB Metals, Part V [1] Preparative and Spectroscopic Studies of the [Hg2I5]-, [Hg2I6]2-and [Hg3I8] 2 -Ions  
 Abstract    The preparations of new compounds, containing the complex anions [Hg2ls] -, [Hg2le] 2-and [Hg3I8] 2 -, are reported. Distorted iodine-bridged configurations are proposed for the complexes in the solid state, utilising analyses, X-ray powder patterns, molar conductance measurements and spectral (IR, UV) data. 
  Reference    Z. Naturforsch. 37b, 646—648 (1982); received November 9 1981 
  Published    1982 
  Keywords    Mercury, Iodomercurates, 3-Picoline, Quinoline, IR Spectra 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-0646.pdf 
 Identifier    ZNB-1982-37b-0646 
 Volume    37 
16Author    Ulrich Müller, Abdel-Fatah Shihada, Kurt DehnickeRequires cookie*
 Title    P(C6H5)4[VOBr4]: Synthese, IR-Spektrum und Kristallstruktur P(C6H5)4[VOBr4]: Synthesis, IR Spectrum and Crystal Structure  
 Abstract    PPh 4 [VOBr4] was prepared by the reaction of PPh4Br with VOBr3 in CH2Br2 solu-tion. The structure of the dark violet crystals was determined with X-ray diffraction. PPli4[VOBr4] crystallizes in the space group P4/n with the lattice constants a = 1275.9 and c = 784.5 pm with two formula units per unit cell. The structure type corresponds to the frequently encountered AsPh4[RuNCl4] type. The VOBr4~ ion forms a square pyramid; the V = O bond has a length of 155 pm. In the IR spectrum, the V —O stretching vibration appears at 922 cm -1 . 
  Reference    Z. Naturforsch. 37b, 699—701 (1982); eingegangen am 29. Januar 1982 
  Published    1982 
  Keywords    Tetraphenylphosphonium Tetrabromooxovanadate(V), Synthesis, IR Spectra, Crystal Structure 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-0699.pdf 
 Identifier    ZNB-1982-37b-0699 
 Volume    37 
17Author    Glycine, GlycineEthyl Ester, Glycylglycine Ethyl, ]. Jurij, Ja Kharitonov, Herbert Bissinger, Eberhard Ambach, Wolfgang BeckRequires cookie*
 Title    IR-Spektren von Platin(II)-Komplexen mit Glycin, Glycin-und Glycylglycinethylester [1] IR-Spectra of Platinum(ll) Complexes with  
 Abstract    The infrared spectra (200-4000 cur 1) of trans-and cw?-Pt(NX2CH2COO)2 (X = H, D), trans-and cis-PtCl2(NH2CH2COOH)2, *rans-PtCl2(NH2CH2C02Et)2, cw-PtCl2(NX2CH2C02Et)2, cw-PtCl2(NX2CH2NXCH2C02Et)2 (X = H, D) and cis-PtY2(NH2CH2NHCH2C02Et)2 (Y = Br, I) including 15 N derivatives have been studied. There is no appreciable change of vibrat ional frequencies for corresponding eis-and trans-complexes which could be attributed to the irans-influence of different ligands. Due to lower symmetry most of the absorptions of the cis-complexes are split into doublets compared with the £rans-compounds. 
  Reference    Z. Naturforsch. 37b, 1034—1040 (1982); eingegangen am 22. März 1982 
  Published    1982 
  Keywords    IR Spectra, Glycine, Glycine Ester Platinum(II) Complexes 
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 Identifier    ZNB-1982-37b-1034 
 Volume    37 
18Author    Rolf Minkwitz, Rüdiger NaßRequires cookie*
 Title    Spektroskopische Untersuchungen an Monofluorammoniumsalzen Spectroscopic Studies on Monofluorammonium Salts  
 Abstract    The NMR, IR and Raman spectra of several NHaF+X -salts are reported. The prepara-tion of NH3F+SO3CI-and NH3F+SO3F-is described. 
  Reference    Z. Naturforsch. 37b, 1558—1563 (1982); eingegangen am 21. Juli 1982 
  Published    1982 
  Keywords    NMR Spectra, Raman Spectra, IR Spectra 
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 Identifier    ZNB-1982-37b-1558 
 Volume    37 
19Author    KarlE. Schwarzhans, Herwig SchottenbergerRequires cookie*
 Title    Ferrocenylen-cobaltocenylenium  
 Abstract    hexafluorophosphat [(h 5 :h 5 '-C10H8)2FeCo] [PF6], ein gemischtkerniger Komplex vom Bis(fulvalen)dimetall-Typus Ferrocenylenecobaltocenyleniumhexafluorophosphate [(h 5 : h 5 '-CioH8)2FeCo][PF6], Ferrocenylenecobaltocenylenium-monochloride and ferrocenylenecobaltocenylenium-hexafluorophosphate were prepared under the aspect of influencing the valence averaging phenomena described for homodinuclear metallofulvalenes. Detected paramagnetism of the monocation is assumed to result from such interactions in dibridged rigid metallocenes. The above cation is characterized by IR, CV, MS, electron microprobe and elemental analyses. 
  Reference    Z. Naturforsch. 38b, 1493—1496 (1983); eingegangen am 28. Juni 1983 
  Published    1983 
  Keywords    Ferrocenylenecobaltocenylenium-monochloride, IR Spectra, MS Spectra 
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 TEI-XML for    default:Reihe_B/38/ZNB-1983-38b-1493.pdf 
 Identifier    ZNB-1983-38b-1493 
 Volume    38 
20Author    Paul Klingelhöfer, Ulrich Müller, HansG. Ünter Hauck, Kurt DehnickeRequires cookie*
 Title    ReCl5 * OPCl3; IR-Spektrum und Kristallstruktur ReCl5 -O PCl3; IR Spectrum and Crystal Structure  
 Abstract    Single crystals of ReCl5 • OPCl3 were obtained by cooling a saturated solution of rheniumpen­ tachloride in phosphorylchloride. It formes black needles, which are extremely sensitive to mois­ ture. In the IR spectrum v(PO) is shifted downwards by 140 cm-1 in comparison with liquid POCl3, indicating coordination via oxygen. The crystal structure was solved and refined from X-ray diffraction data (space group Pnma, four formula units per unit cell, a = 1629, b = 790, c = 877 pm, 902 observed, independent reflexions, R = 0.040). The complex forms discrete molecules ReCl5 • OPC1, with symmetry Cs (m). Bond lengths are Re —O — 214 pm and P —O = 146 pm, the angle Re —O —P is 143°. 
  Reference    Z. Naturforsch. 39b, 135 (1984); eingegangen am 8. September 1983 
  Published    1984 
  Keywords    Preparation, IR Spectra, X-Ray, Rheniumpentachloride Phosphorylchloride Adduct 
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 TEI-XML for    default:Reihe_B/39/ZNB-1984-39b-0135.pdf 
 Identifier    ZNB-1984-39b-0135 
 Volume    39 
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