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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 416-423 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 4-Chloro-1,2,3,5-dithiadiazolium SaltsThe synthesis of 4-chloro-1,2,3,5-dithiadiazolium chloride (9) from SCI2 and either N-cyanosulfur difluoride imide (8) or bis(trimethylsilyl)carbodiimide (12) is described. The analogous dibromide 13 is formed from S2Br2 and 8. The ionic chlorine in 9 may easily be exchanged with the help of silver salts, acids, and Lewis acids yielding ClCN2S2+A- (9a-d, A- = AsF6-, SbCl6-. ½SnCl62-, SO3-). The crystal structure of the hexafluoroarsenate 9a has been determined.
    Notes: Die Synthese von 4-Chlor-1,2,3,5-dithiadiazolium-chlorid (9) aus N-Cyanoschwefeldifluoridimid (8) bzw. aus Bis(trimethylsilyl)carbodiimid (12) und SCI2 wird beschrieben. Das zu 9 analoge Dibromid 13 entsteht aus 8 und S2Br2. Mit Hilfe von Silbersalzen, Säuren und Lewis-Säuren läßt sich das ionisch gebundene Chlor in 9 leicht austauschen unter Bildung von CICN2S2+A- (9a-d, A- = AsF6-, SbCl6-, ½SnCl62-, SO3F-). An dem Hexafluoroarsenat 9a wurde eine Kristallstrukturbestimmung durchgeführt.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0009-2940
    Keywords: Rhodium(I) phosphane complexes ; 14-Electron intermediates ; MO theory, applied ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bis(di-tert-butylphosphanyl)methane Complexes of Rhodium: Geometry, Electronic Structure, and Derivatives of the 14-Electron Fragment [Rh(dtbpm)Cl]. Molecular Structure of Rh(dtbpm)Cl(PMe3)14-Electron fragments [M(PR3)2X] (M = Rh, Ir, X = halogen etc.) are considered to be an important class of highly reactive, coordinatively unsaturated intermediates in many metal-induced stoichiometric or catalytic transformations of organic substrates. As available theoretical data suggest a slightly preferred T-shaped groundstate geometry with a less symmetric cis rather than the usually implied trans phosphane arrangement for such tricoordinate d8-ML3-type systems with monodentate phosphanes PR3, the chemistry of η2-diphosphanylmethane complexes of rhodium with four-membered RhPCP-chelate rings and thus with enforced cis phosphane coordination and anomalously small cis P - Rh - P angles has been studied by theory and by experiment. MO calculations (EH) have been performed both for the model 14-electron system [Rh(dhpm)Cl] (dhpm = diphosphanylmethane, H2P - CH2 - PH2) and for the experimentally accessible fragment [Rh(dhbpm)Cl], where dtbpm is bis(di-tert-butylphosphanyl)-methane, (tBu)2P - CH2 - P(tBu)2. The electronic and geometric structure of these species is described. Employing the unusual ligand dtbpm, tailor-made for stabilizing mononuclear η2- and destabilizing dinuclear μ-diphosphanylmethane coordination, the chloro-bridged dimer [Rh(dtbpm)Cl]2, has been synthesized. In agreement with steric and electronic considerations, its chemistry is dominated by a facile dissociation to monomeric (presumably solvent coordinated) fragments [Rh(dtbpm)Cl], even in benzene, as suggested by molecular mass determinations. Accordingly, by using [Rh(dtbpm)Cl]2 as a starting material, a series of sterically very congested but nevertheless mononuclear, square-planar complexes Rh(dtbpm)Cl(L) (L = CO, PMe3, PPh3, PCy3, pyridine, acrylonitrile) with chelating dtbpm could be readily prepared and fully characterized. The relative stability of these potential alternative precursors of a [Rh(dtbpm)Cl] intermediate towards dissociation of ligands L is reported. The molecular structure of Rh(dtbpm)Cl(PMe3) as the first representative of this class of compounds has been determined by X-ray crystallography.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0009-2940
    Keywords: Magnesium tetrahydridoaluminate ; Magnesium halide tetrahydridoaluminate ; (Organyloxo)magnesium tetrahydridoaluminates ; X-ray structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The molecular structures of XMg(A1H4) · 4 THF (1a, 2, 3a) (X = A1H4, Cl, Br) have been determined by X-ray structural analysis. Each compound possesses a hexacoordinated Mg center and AlH4- groups bound to this center via a single hydride bridge bond. Attempts to prepare ROMg(AlH4) compounds were successful only for sterically demanding groups R (R = CMe3, CPh3, naph, mes, smes). The 2-naphthoxy derivative 7, a compound with the composition (naphO)Mg-(AlH4) · 2.5 THF, is a dimer with a central Mg2O2 ring. One of its two AlH4- groups is terminally bound to one Mg atom, the other bridges the two Mg centers. This structure indicates how AlH4- transfer may occur from ROMg(AlH4) compounds to form Mg(OR)2 and Mg(AlH4)2.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 947-951 
    ISSN: 0009-2940
    Keywords: 6-Aza-nido-decaborane ; 9-(1-Alkenyl)-6-phenyl-6-aza-nido-decaborane ; 1,1-Hydroboration of alkynes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,1-Hydroboration of Alkynes with 6-Aza-nido-decaboranes[1]Alkynes AC≡CR′ (R′ = Me, Bu, tBu, SiMe3), that contain a mobile group A, like H or SiMe3, undergo hydroboration by 6-aza-nido-decaboranes RNB9H11 (1a-c, R = H, Ph, PhCH2) and 1,2-migration of the group A, to give the corresponding 9-(1-alkenyl)-6-aza-nido-decaboranes RNB9H10(CH=CR′A) (2a-h). Ethenes AHC=CH2 (A = SiMe3, SnBu3) are hydroborated by 1a, b as well to form products of the type RNB9H10(CH2CH2A) (3a-c). The alkyne Me3SiC=CH undergoes a hydroboration with 1b twice; the formation of (PhNB9H10)2CHCH2SiMe3 (4) proceeds by a 1,1- and a 1,2-hydroboration step, apparently. The crystal structure analysis of (PhCH2)NB9H10[CH=CMe(SiMe3)] (2e; space group Pl) reveals a (Z configuration of the ethene moiety.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0009-2940
    Keywords: α-Amino acid, α- and β-C-metallated ; Platinum(IV) complexes ; Cobaloxime complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal Complexes of Biologically Important Ligands, LXXXIXPart LXXXVIII: Ref.[1]. .  -  Oxidative Addition of Electrophilic Derivatives of α-Amino Acids to Platinum(II) and Cobalt(I) Complexes: α-Transition-Metallated Amino Acids Herrn Professor Dr. Hans Georg von Schnering zum 65. Geburtstag gewidmet.The addition of methyl α-bromohippurate to PtMe2(bipy) gives the α-metallated amino acid derivative (bipy)-Me2(Br)PtC(H)(NHCOPh)(CO2Me) as a mixture of isomers 1a, b of which the trans adduct 1a was characterized by X-ray diffraction. Methyl α-bromohippurate and N-Boc-O-tosylserine methyl ester are added to [Co(py)(DH)]- (DH = dimethylglyoxime, diphenylglyoxime) to give cobalt(III) complexes 2-5 with a cobalt-carbon bond.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0009-2940
    Keywords: Bis(tetramethylipiperidino)aluminum halides ; Alkoxy((tetramethylpiperidino)aluminum halides ; 27Al-NMR spectra ; Aluminum ; Amides ; Synthetic methods ; Bridging ligands ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-Lithio-2,2,6,6-tetramethylpiperidine [Li(tmp)] reacts with AlX3 (X = Cl, Br) in diethyl ether/ n-hexane solution to generate the products of substitution and ether cleavage, [tmpAl(X)(μ-OEt)], (la, X = Cl; 1b, X = Br). However, when the reaction is allowed to proceed in n-hexane alone, an almost quantitative yield of compounds tmp2AlX (2a, X = Cl; 2b, X = Br; 2c, X = I) is obtained. According to 27AI-NMR spectroscopy, mass spectroscopy, cryoscopy, and X-ray crystal structure determinations, these compounds are monomeric in the solid state, in solution, and in the gas phase. 2b reacts with AgBF4 yielding the fluoride-bridged dimer (tmp2AlF), 2d, as shown by X-ray crystal structure determination.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0009-2940
    Keywords: Benzo-1,3,2-diphosphaborolanes ; Benzo-1,3,2-diphosphaborolane dimmers ; Benzo-1,4,2,3-diphosphadiborinanes ; Rearrangement reaction ; Pentacarbonyl chromium complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of benzo- 1,3,3-diphosphaborolanes C6H4(PR)2BR' (R = H, iPr, SiMe3; R' = R2N, R) has been prepared by several routes and characterized by spectroscopic and - in part - by X-ray diffraction methods. They feature pyramidal P atoms with the substituents in antiperiplanar positions. The P atoms act as coordination sites for the (CO)5Cr fragment. In contrast to the R2N-bearing benzo-1,3,2-diphosphaborolanes, the derivative C6H4(PH)2BCMe3 (4f) dimerizes by additional B-P bond formation to produce a pentacyclic system (4f)2. - The reaction of C6H4(PHNa)2 with B2(NMe2)2Cl2 in THF/hexane yields the acyclic phosphanylborane Me2NB(PH-C6H4PH2)2 (15). However, if C6H4[P(iPr)Li]2 is allowed to react with B2(NMe2)2Cl2, the benzo-1,4,2,3-diphosphadiborinane 13 is obtained, together with its rearrangement product 2-bis(dimethylamino)borylbenzo-1,3,2-diphosphaborolane 14 which dimerizes to (14)2.  -  In contrast, the almost planar ring of the 2,3-dimesitylbenzo-1,4,2,3-diphosphadiborinane (16) possesses P and B atoms with a planar geometry. Short B-B and B-P bonds suggest that this new heterocycle can be regarded as a 6π electron system. Moreover, the benzo-1,5,2,3,4-diphosphatriborepane 18 forms readily forms readily from C6H4(PHNa)2 and Br(Me2N)B-B(N-Me2)-B(NMe2) Br to give a tub-shaped seven-membered C2B3P2 ring system with the P atoms in a pyramidal and the B atoms in a planar environment.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 129 (1996), S. 1335-1344 
    ISSN: 0009-2940
    Keywords: Lithium hydrazide, N-phenyl-N,N′-bis(trimethylsilyl)- ; Lithium hydrazide, N,N′-diphenyl-N′-(trimethylsilyl)- ; Sodium hydrazide, N,N′-diphenyl-N-(trimethylsilyl)- ; Caesium hydrazide, N-phenyl-N′,N′-bis(trimethylsilyl)- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The crystal and molecular structures of a series of N-phenyl-substituted lithium hydrazides were determined in order to investigate possible Li···Ph π interactions. These are pronounced when there are no donor molecules present to solvate the Li centers. An η6-Li···Ph interaction is particularly distinct in tetrameric (Me3Si)2N-N(Ph)Li but also in trimeric Ph2N-N(SiMe3)Li Deprotonation of N,N′ -diphenylhydrazine with butyllithium in ether resulted in the formation of Ph(Li)N-N(Ph)Li · 2 LiNPh2 · 2 OEt2 with phenyl group migration and N-N bond cleavage by a redox process. An increase of the size of the cations, as shown for Ph(Me3-Si)N-N(Ph)Na · NH3 and the caesium salt (Me3-Si)2N-N(Ph)Cs · nTHF, results in increased coordination of the metal ion to the phenyl group. The caesium compound forms a three-dimensional network. Channels along the c axis are partially filled with THF molecules.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0009-2940
    Keywords: Ferrocene, tetrakis(dibromoboryl)- ; Ruthenocene, tetrakis(dibromoboryl)- ; Osmocene, tetrakis(dibromoboryl)- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of metallocenes MCp2 (M = Fe, Ru, Os) with an excess of BBr3 at reflux temperature lead specifically to 1,1′,3,3′-tetrakis(dibromoboryl)metallocenes 3, 7, and 8 in high yield. MeBBr2 and PhBBr2 are less effective borylating agents. X-ray structural analyses of 3, 7, and 8 reveal an increasing tilt of the Br2B groups towards the metal center while retaining the trigonal-planar environment at the boron atoms. This indicates a weak metal-boron interaction of the kind found for carbon-metal interactions in ferrocenyl carbocations.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0009-2940
    Keywords: Tristannylamines ; Tris(trialkylstannyl)amines ; Tris(dialkylhalostannyl)amines ; Sn-N Bond cleavage ; Sn-X-Sn Intramolecular bridges ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tris(triorganylstannyl)amines (R2R'Sn)3N (1, 2) with substituents R = R' = Me, Bu or R = Me and R' = iPr, tBu are obtained by metathesis from R2R'SnX and NaNH2 in liquid ammonia or by transamination of R3SnNMe2 with NH3. Tris(diorga-nylhalostannyl)amines (R2XSn)3N (3) are synthesized by stannazane cleavage of (Me3Sn)3N (1) with R2SnX2. Information from multinuclear magnetic resonance spectra ascertain the planarity of the Sn3N skeleton of type 2 and 3, as well as the relationship between the coupling constants 1J(119Sn15N) and 2J(119Sn117Sn) and the Sn-N bond length as determined by the X-ray structure analysis of 1, 3b and 3r. Compound 3b shows an almost undistorted D3h symmetry with a planar Br3Sn3N skeleton and SnN bond lengths of 1.99 Å, which beside those of 3a are the shortest found so far. According to MNDO approximate and ab initio calculations π interactions between the lone electron pair at the N atom and empty orbitals at the Sn atoms can be excluded. Therefore, the tristan-nylamines discussed here have a trigonal planar nitrogen center with its lone electron pair in a p-type orbital. Further characteristic features of the molecular structures of typ 3 compounds are the intramolecular Sn-X-Sn bridges (X = Cl, Br, I) found in the solid state as well as in solution. The molecular geometries of the tristannylamines are supported by MS fragmentation patterns as well as by infrared and Raman spectra.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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