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21Author    Ekkehard Lindner, Robert SpeidelRequires cookie*
 Title    Neuartige basische Liganden für die homogenkatalytische Methanolcarbonylierung, XXI [1] Synthese und Eigenschaften von (Ether-Phosphan)-Platin-Komplexen Novel Basic Ligands for the Homogenous Catalytic Methanol Carbonylation, XXI [1] Synthesis and Properties of (Ether-Phosphane) Platinum Complexes  
 Abstract    The (ether-phosphane) complexes m -C l2Pt(Ph: P ~ D)2 (2a, b) [D = C H 2C4H 70 (a). C H 2C4H 70 2 (b)] are obtained by reaction of Ph2P ~ D (la , b) with either K2PtCl4 or Cl2Pt(CO D) (C O D = 1,5-cyclooctadiene). Both Cl ^anions are abstracted from 2a, b using A gSbF(1 to give the cationic bischelate complexes [Pt(Ph2P D)2][SbFh]2 (5a, b). The stepwise cleavage and reform a­ tion of Pt —O bonds in (ether-phosphane) platinum complexes is dem onstrated bv the sequence 5a —> [rä -(P h 2P D)(Ph2P ~D)P tC l][S bF 6] (6 a) -* [rra«5-(Ph2P ~ D)2PtC O (C l)][SbF6] (7 a) -* 5a, when 5a, 6 a, and 7a are reacted with KC1. CO, and AgSbF,,, respectively. Reduction of 2a with N aB H 4 results in the form ation of rra/2s-H 2Pt(Ph2P ~ D)2 (4a). In the presence of HC1 2a js re­ formed. Excess N aBH 4 or heating of 4a yields the bischelate platinum(O) complex Pt(P h: P D)2 (3a), which is also jso lated by reduction of 2a with sodium amalgam. A general method for obtaining P t(P h2P D)2 (3 a —c) [D = C H 2C H 2O C H , (c)] is the substitution of C O D in P t(C O D)2 by the ether-phosphanes l a —c. The structures and bonding properties of the com pounds 2 —7 are discussed on the basis of their 31P {1H } NMR and IR spectra. 
  Reference    Z. Naturforsch. 44b, 437—443 (1989); eingegangen am 20. D ezem ber 1988 
  Published    1989 
  Keywords    Ether-Phosphanes Platinum Complexes, 3iP {'H} NMR Spectra, IR Spectra 
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 TEI-XML for    default:Reihe_B/44/ZNB-1989-44b-0437.pdf 
 Identifier    ZNB-1989-44b-0437 
 Volume    44 
22Author    Reiner Figge, Claus Friebel, U. Te Patt-Siebel, Ulrich Müller, Kurt DehnickeRequires cookie*
 Title    Nitridokomplexe von Molybdän(V); Synthesen, IR-und EPR-Spektren. Die Kristallstruktur von [Na(15-Krone-5)Na(THF)]2[MoNCI3 THF]4-2THF Nitrido Complexes of M olybdenum (V ); Syntheses, IR , and EPR Spectra. Crystal Structure of [N a(15-Crow n-5)N a(TH F)]2[MoNCl3-THF]4-2T H F  
 Abstract    Nitrido C om plexes o f M olyb denu m (V), 
  Reference    Z. Naturforsch. 44b, 1377—1384 (1989); eingegangen am 30. Mai 1989 
  Published    1989 
  Keywords    Syntheses, IR Spectra, EPR Spectra, Crystal Structure 
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 TEI-XML for    default:Reihe_B/44/ZNB-1989-44b-1377.pdf 
 Identifier    ZNB-1989-44b-1377 
 Volume    44 
23Author    Michael Schäfer, Jürgen Pebler, Beatrice Borgsen, Frank Weller, K. Urt DehnickeRequires cookie*
 Title    21Sb-Mössbauer-spektroskopische und strukturchemische Untersuchungen an Kronenetherkomplexen SbX3(15-Krone-5) mit X = F, Cl, Br, I. Eine Analyse der Orbitalbesetzungszahlen 12lSb-M össbauer-Spectroscopic and Structural Investigations on Crown Ether Complexes SbX3(15-Crown-5) with X = F, Cl, Br, I. A Population Analysis Crown Ether C om plexes SbX3(15-crown-5)  
 Abstract    The crown ether complexes SbX3(15-crown-5) with X = F, Cl, Br, and I have been prepared by reactions o f 15-crown-5 with the corresponding antimony trihalides in acetonitrile solu­ tions. The com pounds were characterized by IR spectroscopy as well as by l21Sb-M össbauer spectroscopy. A m ethod o f orbital population analysis utilizing both M össbauer isomer shifts and quadrupole coupling has been developed for Sb(III) antimony halides and their crown ether com plexes. SbF 3(l 5-crown-5) was also characterized by an X-ray structure determination: Space group P 2 ,/«, Z = 4, 3628 observed unique reflexions, R = 0.032. Lattice dim ensions at 19 °C: a = 891.54(6), b = 1277.26(6), c = 1277.66(7) pm, ß = 95.029(4)3. The com plex has a molecular structure in which the antimony atom is surrounded by three F-atom s with mean bond lengths o f 192.4 pm and by the five oxygen atom s o f the crown ether molecule with mean bond lengths o f 293.9 pm. 
  Reference    Z. Naturforsch. 45b, 1243—1250 (1990); eingegangen am 5. März/9. Mai 1990 
  Published    1990 
  Keywords    Syntheses, IR Spectra, 12lSb-M össbauer Spectra, Crystal Structure 
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 TEI-XML for    default:Reihe_B/45/ZNB-1990-45b-1243.pdf 
 Identifier    ZNB-1990-45b-1243 
 Volume    45 
24Author    Gabriele Schatte, Helge WillnerRequires cookie*
 Title    Die Wechselwirkung von N 3F mit Lewis-Säuren und HF. N 3F als möglicher Vorläufer für die Synthese von N 3+-Salzen The Interaction of N 3F with Lewis-Acids and HF. N 3F as Possible Precursor for the Synthesis of N 3+ Salts  
 Abstract    Triazadienyl fluoride, N 3F, forms stable adducts with BF3 and AsF5 at low temperatures, as demonstrated by infrared measurements. The Lewis acids are bonded to the Na-atom of N 3F, as deduced from the data for 15N-isotopically enriched N 3F. The basicity of N 3F is comparable to that of ethine and ethene, according to the HF stretching frequency of the N 3F/HF complex isolated in an argon matrix. Despite the low NF bond energy (<150 kJ/mol), abstraction of the fluoride ion and formation of an N 3+ salt was not possible. The different behavior of N 3F and C1N3 towards Lewis acids is discussed. 
  Reference    Z. Naturforsch. 46b, 483—489 (1991); eingegangen am 3. September 1990 
  Published    1991 
  Keywords    Triazadienyl Fluoride, IR Spectra, Lewis Acids, Proton Affinity 
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 TEI-XML for    default:Reihe_B/46/ZNB-1991-46b-0483.pdf 
 Identifier    ZNB-1991-46b-0483 
 Volume    46 
25Author    Rolf Minkwitz, Volker Gerhard, FrauRequires cookie*
 Title    Über Dimethylhaloniumsalze -CH3C1CH3+M F6 , CH3BrCH3+M F6 , CH3ICH3+MF6" -und Dimethylmethylendiiodoniumsalze CH3ICH2ICH32+(M F6 )2 (M = As, Sb)  
 Abstract    The dimethylhalonium salts (C H 3)2X +A~ (X = Cl, Br, I; A " = A sF 6-, SbF6~, Sb2F n ~) are synthesized by methylation o f the corresponding methylhalides C H 3X or dihalomethanes C H 2C12 and CH2Br2 in the system S 0 2/C H 3F /M F 5. The analogous reaction o f C H 2I2 results in the formation o f dimethylmethylendiiodonium hexafluorometallates C H 3IC H ,IC H 32+(M F 6")2 (M = As, Sb). The salts are characterized by Raman-, IR-and N M R-spectroscopy. 
  Reference    Z. Naturforsch. 46b, 561—5 (1991); eingegangen am 21. Juni 1990 
  Published    1991 
  Keywords    Preparation, Raman Spectra, IR Spectra, N M R Spectra 
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 TEI-XML for    default:Reihe_B/46/ZNB-1991-46b-0561.pdf 
 Identifier    ZNB-1991-46b-0561 
 Volume    46 
26Author    R. Olf Minkwitz, VolkerG. ErhardRequires cookie*
 Title    Über die Reaktionen der Halogene Cl2, Br2 und I2 mit CH3O S O +M F6 (M = As, Sb)  
 Abstract    Chlorine reacts with C H 3O SO +M F6" (M = As, Sb) at 298 K to form AsC14 +A sF 6" and SbCl4 +Sb2Cl2F9~, respectively. The analogous reactions with bromine at 233 K result in the formation o f (C H 3)2 Br+A sF 6~ and Sb2F,,~. With iodine, the new methyliodonium salts (C H 3 I2)n"+(M F 6~)n (M = As, Sb) with yet unknown constitution are obtained. 
  Reference    Z. Naturforsch. 46b, 1470—1472 (1991); eingegangen am 11. März 1991 
  Published    1991 
  Keywords    Preparation, IR Spectra, N M R Spectra 
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 TEI-XML for    default:Reihe_B/46/ZNB-1991-46b-1470.pdf 
 Identifier    ZNB-1991-46b-1470 
 Volume    46 
27Author    Rene Wollert, SigridW. Ocadlo, K. Urt Dehnicke, Helmut Goesmann, Dieter FenskeRequires cookie*
 Title    Die Kristallstrukturen von (PPh4)2 [TiCl3 (NSiMe3) ] 2 * CH3CN und (PPh4)2 [TiCl4(OSPCl2) ] 2 The Crystal Structures of (PPh4)2[TiCl3(NSiM e3)]2 -C H 3CN and (PPh4)2[TiCl4(OSPCl2)]2  
 Abstract    (PPh4)2[TiCl3(N SiM e3)]2 C H 3CN has been prepared from [TiCl^NSiM ej)]^ with PPh4Cl in acetonitrile solution as yellow crystals. The com pound crystallizes in the triclinic space group P 1 with one formula unit per unit cell, 3447 observed unique reflections, R = 0.053. Lattice dimensions at 200 K: a = 1030(1), b = 1253(1), c = 1374(1) pm, a = 77.46(8)°, ß = 73.93(8)°, y = 69.99(9)°. The structure consists o f PPh4+ ions and centrosymmetric dimeric anions [TiCl3(N SiM e3)]2~, in which pentacoordinate titanium atom s are associated via the nitrogen atoms o f the silylimido groups. (PPh4)2[TiCl4(OSPCl2)]2 has been prepared by the reaction o f PPh^fOSPClJ with titanium tetrachloride in C H 2C12 solution as orange crystals. (Space group P I , Z = 1, 3242 observed unique reflections, R = 0.033). Lattice dim ensions at 193 K: a = 1114.8(2), b = 1190.6(2), c = 1218.7(2) pm, a = 72.18(1)°, ß = 85.45(1)°, y = 69.19(1)°. The structure consists o f PPh4+ ions and centrosymmetric dimeric anions [TiCl4(O SPCl2)]^~, in which hexacoordinate titanium atom s are associated via two chlorine atoms. The OSPCl2_ group is coordinated via the oxygen atom. 
  Reference    Z. Naturforsch. 47b, 1386—1392 (1992); eingegangen am 9. März 1992 
  Published    1992 
  Keywords    Dimeric Titanium Complexes, Synthesis, IR Spectra, Crystal Structure 
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 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-1386.pdf 
 Identifier    ZNB-1992-47b-1386 
 Volume    47 
28Author    Michael Plate, Peter Hofacker, WernerM. Assa, Birgit Schwarz, Bernhard Neumüller, Kurt DehnickeRequires cookie*
 Title    Synthese und Kristallstrukturen der Wolfram(VI)-Alkinkomplexe |WCl4(P h -C = C -I)(T H F )l und [WCl4( P h -C = C -T e -C 4H9)(THF)| Synthesis and Crystal Structures o f the Tungsten(VI) Alkyne Complexes [WCl4(P h -C = C -I)(T H F )] and [WCl4( P h -C = C -T e -C 4H 9)(THF)]  
 Abstract    [WCl4(P h -C = C -I)(T H F)] has been prepared by the reaction o f mrns-[WCl4(SEt2)2] with P h -C = C -I in TH F solution, whereas [WCl4(P h -C = C -T e -n C 4H 9)(THF)] has been syn­ thesized by the reaction o f P h -C = C -T e -« C 4H 9 with tungsten hexacloride in the presence o f C2C14 and THF. Both complexes were characterized by IR spectroscopy and by crystal struc­ ture determinations. [WCl4(P h -C = C -I)(T H F)]: Space group P 2,/c, Z = 4, 2617 observed unique reflections, R = 0.064. Lattice dimensions at -7 0 °C: a = 1518.2(3), b = 714.5(1), c = 1540.0(3) pm, ß = 90.09(3)°. [WCl4(P h -C = C -T e -« C 4H9)(TH F)]. Space group P 1, Z = 2, 3911 observed unique reflec­ tions, R = 0.067. Lattice dimensions at 20 °C: a = 844.0(3), b = 974.6(4), c = 1002.4(3) pm, a = 76.00(4),/? = 105.14(1), y = 82.03(3)°. Both complexes have molecular structures, in which the tungsten atom s are seven-coordi­ nate by four chlorine ligands, by the two alkyne carbon atom s, and in trans position to the latter by the oxygen atom o f the T H F molecule. The WC bond lengths are 198 and 200(1) in the telluro complex and 206 and 196(1) pm in the iodine derivative. 
  Reference    Z. Naturforsch. 48b, 1105—1111 (1993); eingegangen am 21. April 1993 
  Published    1993 
  Keywords    Tungsten Alkyne Complexes, Synthesis, IR Spectra, Crystal Structure 
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 TEI-XML for    default:Reihe_B/48/ZNB-1993-48b-1105.pdf 
 Identifier    ZNB-1993-48b-1105 
 Volume    48 
29Author    Frank Weller, Fritjof Schmock, Kurt Dehnicke, Kurt Findeisen Bayer-WerkRequires cookie*
 Title    Synthese, IR-Spektrum und Kristallstruktur von 1.3.5-Trichlortriazinium-hexachloroantimonat, [HC3N3C13]SbCl6 Synthesis, IR Spectrum and Crystal Structure of 1.3.5-Trichlortriazinium Hexachloroantim onate, [HC3N3Cl3]SbCl6  
 Abstract    ,3,5-Trichlortriazinium hexachloroantimonate has been prepared by the reaction of CCl2 = N-COCl with antimony pentachloride in boiling dichloromethane. The compound was characterized by IR spectroscopy and by a crystal structure determination. [HC3N3Cl3]SbCl6 crystallizes in the monoclinic space group P 2 Jn with four formula units per unit cell. 2503 observed unique reflections, R = 0.029. Lattice dimensions at 19 °C: a = 1314.1(1), b = 958.2(1), c = 1329.1(1) pm, ß = 117.113(5)°). The compound forms ion pairs via a linear N -H • • • Cl bridge, thus distorting the SbCl6~ ion from octahedral geometry. The C3N3 skeleton of the [HC3N3C13]+ ion is nearly planar, but the hydrogen atom lies about 30 pm out of this plane. 
  Reference    Z. Naturforsch. 49b, 360—364 (1994); eingegangen am 3. November 1993 1.3. 
  Published    1994 
  Keywords    5-Trichlortriazinium Salt, Synthesis, IR Spectra, Crystal Structure 1 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-0360.pdf 
 Identifier    ZNB-1994-49b-0360 
 Volume    49 
30Author    Z. NaturforschRequires cookie*
 Abstract    Single crystals of (Me3Sn)3CCN were obtained by the reaction of tris(trimethylstannyl)amine with boiling acetonitrile in the presence of potas­ sium fluoride and trimethylarsane. The compound has been characterized by IR spectroscopy and by a crystal structure determination. Space group 
  Reference    Z. Naturforsch. 52b, 145—148 (1997); eingegangen am 7. Oktober 1996 
  Published    1997 
  Keywords    Tin Compound, Synthesis, IR Spectra, Crystal Structure 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0145_n.pdf 
 Identifier    ZNB-1997-52b-0145_n 
 Volume    52 
31Author    N.M U Rq, U. Iza3, S.G M AncaaRequires cookie*
 Title    On the Incorporation o f Li(I) into the Fluoroapatite Lattice  
 Abstract    a Instituto de Q ufm ica A nalftica, Facultad de Bioqufm ica, Q ufm ica y Farmacia, U niversidad N acional de Tucum än, 4000-Tucum an, A rgen tina b C entro de Q ufm ica Inorgänica (C E Q U I N O R), Facultad de C iencias Exactas, U n iversidad N acional de La Plata, C. C orreo 962, In attem pts to incorporate the L i(I) cation into the C a(II) position s o f the fluoroapatite lattice it has been sh ow n that the unit cell b eco m es increasingly distorted with the increase o f lithium concentration. C rystallographic data have been obtained from X-ray pow d er data. The infrared spectra o f th ese su bstitu ted apatites sh ow that the Li(I) incorporation has a n egligible effect on the strength o f the P-O bonds. 
  Reference    Z. Naturforsch. 52b, 1281 (1997); received July 2 1997 
  Published    1997 
  Keywords    Lithium, F luoroapatite, Crystal D ata, IR Spectra 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-1281_n.pdf 
 Identifier    ZNB-1997-52b-1281_n 
 Volume    52 
32Author    Wolfgang Beck, ThomasM. KlapötkeRequires cookie*
 Title    and IR Frequencies of the Anionic Fulminate Complexes [Co(CNO)6]3-, [Ni(CNO)4]2-, [Zn(CNO)4]2-, [Pt(CNO)4]2", [Au(CNO)2] ' and [Hg(CNO)4]2  
 Abstract    The structural parameters and IR frequencies of the following anionic fulminate complexes were computed at the density functional BPW91 level of theory using a 6-31++G(2d) basis for C, N, O, Co, Ni, and Zn and quasi-relativistic ECP60MWB core potentials for Pt, Au and Hg: [Co(CNO)6]3-(Oh), [Ni(CNO)4]2-(D 4h), [Zn(CNO)4]2-(Td), [Pt(C N 04]2-(D 4h), [Au(CNO)2]~ (£>xh) and [Hg(CNO)4]2-(Td). The structures were optimised within the symmetries stated above and were found to represent true minima (number of imaginary frequencies, NIMAG = 0). The agreement between the calcu­ lated structural parameters and characteristic asymmetric and symmetric CNO stretching fre­ quencies is very good for all complexes. 
  Reference    Z. Naturforsch. 56b, 1376—1378 (2001); received October 16 2001 
  Published    2001 
  Keywords    DFT Calculations, Fulminate Complexes, IR Spectra 
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 TEI-XML for    default:Reihe_B/56/ZNB-2001-56b-1376_n.pdf 
 Identifier    ZNB-2001-56b-1376_n 
 Volume    56 
33Author    M. Maeda, T. Ito, M. Hori, G. JohanssonRequires cookie*
 Title    The Structure of Zinc Chloride Complexes in Aqueous Solution  
 Abstract    The structure of zinc chloride complexes with different ratios of chloride to zinc, formed in concentrated ZnCl 2 aqueous solutions, were determined from large-angle X-ray scattering using concentrations of the chloride complexes estimated by complementary Raman spectroscopic mea-surements. The highest chloro complex, [ZnCl 4 ] 2 ~, is tetrahedral with a Zn-Cl bond length of 2.294(4) Ä. The trichloro complex, [ZnCl 3 ]~, which coordinates one water molecule, is pyramidal with the Cl-Zn-Cl angle 111°. The Zn-Cl and the Zn-H 2 0 bonds are 2.282(4) and 1.9 A, respec-tively. The two lower complexes, [ZnCl 2 ] and [ZnCl] + , cannot be separated by Raman spectra. o The average Zn-Cl distance in these complexes is 2.24 Ä, and the average Zn-H 2 Ö distance is 1.9 A. In [Zn(H 2 0) 6 ] 2+ the Zn-H 2 0 distance is 2.15 Ä. of zinc (II) chloride complexes; structure of hydrated non-complexed zinc (II) ion. 
  Reference    Z. Naturforsch. 51a, 63—70 (1996); received November 7 1995 
  Published    1996 
  Keywords    X-ray diffraction, Raman spectra, IR spectra, structures 
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 TEI-XML for    default:Reihe_A/51/ZNA-1996-51a-0063.pdf 
 Identifier    ZNA-1996-51a-0063 
 Volume    51 
34Author    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 
35Author    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 
36Author    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 
37Author    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 
38Author    Römer, H. Scholl, H. Budzikiewicz, H. Korth, G. PulvererRequires cookie*
 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 
39Author    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 
40Author    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