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  • Electronic Resource  (3,613)
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  • 1990-1994  (3,613)
  • Inorganic Chemistry  (3,613)
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  • Electronic Resource  (3,613)
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  • 201
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1263-1267 
    ISSN: 0009-2940
    Keywords: Photochemistry ; Stereoselective bromination ; Deoxygenation ; Allyl-Cyclopropyl ring closure ; 2D-NMR ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of Medium and Large Rings, XXXVI.  -  Synthesis of a Bridged Bicyclo[2.1.0]pentane Derivative with inside ConfigurationDihydrocyclobutafurans 4 (H instead of Br) are reactive intermediates in the photochemical rearrangement of 3,6-hexanooxepine-4,5-dicarboxylic esters. The synthesis of the bromo derivative 4 was achieved by irradiation of the epoxyoxepine 1 followed by a regio- and stereoselective NBS bromination of 2 and deoxygenation of 3 with tungsten hexachloride/n-butyllithium. Treatment of the allylic bromide 4 with sodium methoxide gave surprisingly the title compound 5. The structure of 5 was established by thorough NMR analysis.
    Additional Material: 1 Ill.
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  • 202
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1275-1281 
    ISSN: 0009-2940
    Keywords: Ketenes (dimeric) ; reactions with nucleophiles and electrophiles ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The title lactone 2 acylates a variety of amines including phenylalanine, sterically hindered alcohols, and phenols. With activated non-enolizable carbonyl compounds, bis-spiro 6-membered β-keto lactones are formed. Oxidative rearrangement of 2 affords bis-spiro lactones 12 and 13.
    Additional Material: 3 Tab.
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  • 203
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1269-1274 
    ISSN: 0009-2940
    Keywords: Ketene cycloadditions ; Cycloheptadienones ; Carbocations ; Rearrangements ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of ketenes 1a or 1b with diene 2 in the presence of trifluoromethanesulfonic acid providing the cycloheptadienones 5a and 5b constitutes the first example of an acid-induced ketene/diene «cycloaddition». The thermal [2 + 2] cycloadducts, bicyclo[3.2.0]hept-2-en-6-ones 9, are not intermediates in the acid-catalyzed reaction since they rearrange under acidic conditions to the tetralinone derivatives 10. The acid-catalyzed «cycloaddition» was mechanistically investigated and the scope of the reaction explored.
    Additional Material: 1 Ill.
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  • 204
    ISSN: 0009-2940
    Keywords: (Aminomethylene)cyanoacetate, ethyl, derivatives ; Coordination polymers, 1D ; Self-organization, spontaneous ; Copper complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of a solution of copper(II) acetate in methanol with ethyl (aminomethylene)cyanoacetate derivatives 10 (H2L4) or 13 (H2L5) yields the corresponding 1D-coordination polymers 11 ([CuL4]∞ and 14 ([CuL5]∞, respectively. The products are insoluble in non-coordinating solvents and thermally highly stable. The structures of 11 and 14 have been established by X-ray diffraction. The one-dimensional coordination polymers 11 and 14 have different geometries, depending on the lateral group of the ligands.
    Additional Material: 3 Ill.
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  • 205
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1295-1303 
    ISSN: 0009-2940
    Keywords: Imines ; Iminium salts ; 3-Trifloxypropeniminium salts ; Propyniminium salts ; Cyclization reactions ; Azacyclobutadiene ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The imines 5 and 11 react with 3-trifloxypropeniminium triflates 1a-d to afford the heterocyclic iminium salts 8, 9, 13, 15, and 17, respectively, or the propeniminium salt 21. Propyniminium triflates 22, 24 react with imines by initial conjugated addition, followed by a reaction sequence analogous to the one observed for the reactions of 1a-d with imines. Thus, salt 22 and aldimine 5b yield the propeniminium salt 21, while 24 reacts with tri-tert-butylazete 25 to afford the semicyclic vinamidinium salt 28. A crystal structure analysis of 28 is performed.
    Additional Material: 2 Ill.
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  • 206
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1287-1293 
    ISSN: 0009-2940
    Keywords: Ynamines, N,N-bis(trimethylsilyl)- ; Cycloaddition reactions ; Cyclopropenes ; Furans ; Ketenes ; Cyclobutenones ; Allenylcarboxamides ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N,N-Bis(trimethylsilyl)ynamines 1 react with dimethyl acetylenedicarboxylate (2) in a molar ratio of 1:2 to afford 3-cyclopropenylfurans 3. Configuration and conformation of 3a are confirmed by X-ray crystallography. Addition of a further mol of 1 furnishes the fumarates 4. With ketenes 5 (5c, d are prepared in situ) a competition between the formation of cyclic butenone derivatives 6 and allenic imidates 7 is observed, depending on the substitution pattern of 1. After hydrolytic workup, the corresponding amides 10 or the vinylogous amides 9 are obtained in good yield. These experiments indicate that the silylated ynamines 1 show a completely different, more selective reactivity towards dimethyl acetylenedicarboxylate compared to N,N-dialkyl-substituted ynamines, yielding furan derivatives instead of anilines. Towards ketenes, however, a similar cycloaddition reactivity as for N,N-dialkylynamines is observed.
    Additional Material: 1 Ill.
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  • 207
    ISSN: 0009-2940
    Keywords: Radicals ; Cyclobutanes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical-Type Cyclization of Dienes, IX. - On the Stereoselectivity of the Radical 4-exo-trig-Cyclization of Optically Active Ethyl (2E)-6-Oxohex-2-enoates with Samarium(II) IodideEthyl (5R, 2E)-5-(benzyloxy)-4,4-dimethyl-6-oxohex-2-enoate (9) was prepared from (R)-(-)-pantolactone (3) by a series of straightforward reactions. The reaction of 9 with samarium(II) iodide produces enantiomerically pure ethyl (1S,3R,4R)-(-)-[3-(benzyloxy)-4-hydroxy-2,2-dimethylcyclo-butyl]acetate (10) in 60% yield. The absolute configuration at C-1 and C-3 was confirmed by the conversion of 10 to the crystalline 15a, whose absolute configuration is known from its synthesis from (1S,5S)-( + )-α-pinene (12). The configuration of the hydroxy group at C-4 in 10 was determined from NOE studies on the epimiric 17. The radical 4-exo-trig-cyclization of optically active (2E)-6-oxohex-2-enoates with samarium(II) iodide opens a new pathway to enantiomerically pure cyclobutanol and cyclobutanone derivatives, which are of interest as building blocks in natural products synthesis.
    Additional Material: 1 Tab.
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  • 208
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1311-1316 
    ISSN: 0009-2940
    Keywords: 1-Iodoalkylmagnesium reagents ; Stability, configurational ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Iodoalkylmagnesium species were generated by reaction of 3-oxygenated 1,1-diiodoalkanes with isopropylmagnesium halides at -78%C. The resulting magnesium carbenoids were found to be configurationally stable at temperatures up to -20%C and were trapped by benzaldehyde or allyl iodide at low temperatures. Stereoselectivity on exchange of the diastereotopic iodine atoms in 3 was found to be low.
    Additional Material: 3 Tab.
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  • 209
    ISSN: 0009-2940
    Keywords: Allylamine nickel complexes ; Allylamine cobalt complexes ; 2D NMR, TOCSY ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 16-Electron complexes of zerovalent nickel with diallylamines, Ni[(C3H5)2NR]L [1, 2: L = P(CH3)3, R = CH3, C6H5; 3: L = P(C6H5)3, R = CH3] and [NiP(CH3)3]2CH2[N(C3H5)2]2 (4), were synthesized by reduction of NiCl2L2 with magnesium in tetrahydrofuran. NiCl(η3-C3H5)[P(CH3)3]2 (5), a low-yield byproduct, was also obtained in high yield from NiL4 and C3H5Cl. With triallylamine as starting material complexes Ni[(C3H5)3N]L [6: L = P(CH3)3; 7: L = P(C6H5)3] were generated exhibiting η6- and η4-olefin coordination, respectively. 17-electron cobalt(O) compounds Co[(C3H5)2NR](PMe3)2 (8, 9: R = CH3, C6H5) were obtained by reaction of Co(cyclo-C5H8)(PMe3)3 with the corresponding diallylamine, while CoR(PMe3)4 (R = CH3, C6H5) reacted with N,N-diallylaniline to give diagmagnetic Co[(η3-C3H4)(η2-C3H5)NC6H5](PMe3)2, (10). The coordination mode of allylic functions was deduced from IR, ESR and especially 1H- and 13C-NMR spectra including 2D-NMR experiments.
    Additional Material: 1 Ill.
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  • 210
    ISSN: 0009-2940
    Keywords: Alkynylnickel halides ; Nickel complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidative Linear Trimerization of Alkynyl Groups in (Trimethylphosphane)nickel Complexes: Structures and the Role of Ligand-Rich Precursors NiX(C≡CR)(PMe3)n (n = 2-4)Oxidative additions of 1-halogenoalkynes XC≡CR; to Ni(PMe3)4 afford high yields of pentacoordinate ionic alkynylnickel compounds [Ni(C≡CR)(PMe3)4]+X- [R = SiMe3, X = I (1); R = CMe3, X = I (2), Br (3); R = SiEt3, X = I (6), Br (7); R = SiiPr3, X = I (10), Br (11), R = Ph, X = I (21), Br (22)] or complex molecules Ni(C≡CR)X(PMe3)3 [R = SiPh3, X = I (14), Br (15); R = Ph, X = I (19), Br (20)]. Dissociation of trimethylphosphane gives square planar trans-Ni(C≡CR)X-(PMe3)2 [R = CMe3, X = Br (4), Cl (5); R = SiEt3, X = Br (8), Cl (9); R = SiiPr3, X = Br (12), Cl (13); R = SiPh3, X = I (16), Br (17), Cl (18); R = Ph, X = I (23), Br (24), Cl (25)] but with R = SiR'3, X = I the title reaction dominates with formation of trans-Ni[C(C≡CR)=CR(C≡CR)]I(PMe3)2 [R = CMe3 (26), SiEt3 (29), SiiPr3 (32)]. Thermal activation is necessary in order to obtain trans-Ni[C≡CR)=CR(C≡CR)]X(PMe3)2 [R = CMe3, X = Br (27), Cl (28); R = SiEt3, X = Br (30), Cl (31); R = SiiPr3, X = Br (33), Cl (34)], while only thermal decomposition is observed with trans-Ni(C≡CR)X(PMe3)2 (R = Ph, SiPh3). Examples for both types of reactivity including structural data are given: trans-Ni(C≡CRSiMe3)Br(PMe3)2 and 25 crystallize in the space group P1. Pentacoordinate 19 (space group P21) adopts a trigonal pipyramid of ligand donor atoms with equatorial phenylethynyl and iodo ligands.
    Additional Material: 5 Ill.
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  • 211
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. A-105 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 212
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1811-1813 
    ISSN: 0009-2940
    Keywords: Vinylferrocene ; Palladium-catalyzed couplin ; (Ferrocenylvinyl)arenes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: (Ferrocenylvinyl)arenes 3, 5, and 7 are obtained from vinylferrocene (1) and substituted aromatic and heteroaromatic halides by palladium-catalyzed Heck-type reactions. Up to three ferrocene units are introduced in one step by the multi-fold reaction of 1,2-dibromo- (4) or 1,3,5-tribromobenzene (6) with 1. The first crystal structure of a bis(ferrocenylvinyl)benzene chromophore (5) is reported.
    Additional Material: 1 Ill.
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  • 213
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1851-1856 
    ISSN: 0009-2940
    Keywords: Grignard reagents, 1,3-di- ; Titanocene ; Zirconocene ; Platinum, complexes of ; Rhodium, complexes of ; Iridium, complexes of ; Metallacycles ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Five 1,8-naphthalenediyl transition metal compounds 2 were prepared by treating either 1,8-naphthalenediylmagnesium (1) or 1,8-dilithionaphthalene with the appropriate transition metal dichloride LnMCl2: LnM = Cp2Ti (2a), (PEt3)2Pt (2b), Cp* PPh3Rh (2c), Cp* PPh3Ir (2d), or Cp*2Zr (2e). The resulting metallacycles were characterized by NMR and mass spectrometry. X-ray crystal structure analyses were performed for (1,8-naphthalenediyl)titanocene (2a) and (1,8-naphthalenediyl)bis(triethylphosphane)platinum (2b). Despite the strain induced by the four-membered metal-containing rings, the naphthalene units show remarkably small distortions.
    Additional Material: 2 Ill.
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  • 214
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1871-1875 
    ISSN: 0009-2940
    Keywords: Oxidation by HOF ; Hypofluorous acid ; Addition compounds of HOF and HF with acetonitrile ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidation Reactions with HOF and Adducts of HOF and HF with AcetonitrileIn acetonitrile solution HOF oxides CF3SSCF3 via CF3S(O)nSCF3 (n = 1, 2) to yield [CF3S(O)2]2O. Analogously, CF3Se(O)OH and CF3SeX (X = Cl, Br) are oxidized via CF3Se(VI) intermediates to provide finally [CF3Se(O)2]2O. With CH3CN at low temperatures HOF and HF form 1:1 adducts, whose structures have been elucidated by low-temperature X-ray structure analysis. Additional proof for the formation of CH3CN · HF in the liquid phase is provided.
    Additional Material: 3 Ill.
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  • 215
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1901-1908 
    ISSN: 0009-2940
    Keywords: Diborane(4) dianion, 1,2-bis(dimethylamino)-1,2-di-9-fluorenyl- ; Li, Na, K, Cs salts ; Ca, Ba salts ; Main group metallocenes ; Hetero-ansa-bridged metallocenes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,2-Bis(dimethylamino)-1,2-di-9-fluorenyldiborane(4) (1) is doubly metallated with group 1 and 2 metals to yield metal 1,2-bis(dimethylamino)-1,2-di-9-fluorenyldiborate(4) 2-Li to 2-Ba. The conformations of these compounds in solution are investigated by NMR spectroscopy, and the solid-state structures of 2-Li · 5 THF, 2-K · 4 THF, 2-K · 2 DME, and 2-Ca · 2 THF are determined by X-ray diffraction. All four structures can be described as main group metallocenes. The potassium derivatives form contact ion pairs, leading to polymeric chain-like structures. In contrast, 2-Li · 5 THF exhibits the rare combination of a contact ion pair with a solventseparated ion pair, giving the monomeric structure [Li(THF)4][(fl2B2(NMe2)2)Li · THF]. 2-Ca · 2 THF, which is also monomeric, adapts a severely distorted geometry.
    Additional Material: 5 Ill.
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  • 216
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 2369-2372 
    ISSN: 0009-2940
    Keywords: Cyclopentadienyl complexes ; Carbene complexes ; Samarium(II) compounds ; Ytterbium(II) compounds ; Lanthanides, organo- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organometallic Compounds of the Lanthanides, 91[1]. - Carbene Complexes of Divalent Samarium and Ytterbium(Imidazol-2-ylidene)lanthanide adducts (C5Me4Et)2Sm-CN-(iPr)CMe=CMeN(iPr) (5b), (C5Me5)2Yb-CN(Me)CMe=CMeN(Me) (6a), (C5Me5)2Yb-CN(iPr)CMe=CMeN(iPr) (6b), and (C5H3tBu2)2Yb-CN(Me)CMe=CMeN(Me) (7a) are obtained from 1,3,4,5-tetramethyl-imidazol-2-ylidene (4a) or 1,4-diisopropyl-2,3-dimethylimidazol-2-ylidene (4b) and (C5Me4Et)2Sm(THF) (1), (C5Me5)2Yb(THF) (2), or (C5H3-tBu2)2Yb(THF) (3). The molecular structure of the ytterbium carbene complex 7a has been determined by X-ray diffraction.
    Additional Material: 1 Ill.
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  • 217
    ISSN: 0009-2940
    Keywords: Dinuclear palladium(II) complexes ; Bis(1-methylimidazol-2-yl) ketone ; Pyridine-2-thione ; Pyrimidine-2-thione ; 4-Imidazoline-2-thione, 1-methyl- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three novel dinuclear palladium(II) complexes with the chelating ligand bis(1-methylimidazol-2-yl) ketone (bmik) as well as pyridine-2-thiolate (pyt), pyrimidine-2-thiolate (pymt), and 1-methylimidazole-2-thiolate (meimt) as bridging secondary ligands were prepared by reactions of diaqua[bis(1-methylimidazol-2-yl) ketone]palladium(II) nitrate with the ligands in aqueous solution. The thiolates bridge the two metal atoms in the μ-N,S mode. The structures of the following compounds were analyzed by single crystal X-ray diffraction: Bis(μ-pyridine-2-thiolato-N,S)-bis{[bis(1-methyl-imidazol-2-yl) ketone]palladium(II)}nitrate [Pd2(bmik)2-(pyt)2](NO3)2 · 5 H2O (1), bis(μ-pyrimidine-2-thiolato-N1,S)- bis{[bis(1-methylimidazol-2-yl) ketone]palladium(II)} nitrate [Pd2(bmik)2(pymt)2](NO3)2 · 5 H2O (2), and bis(μ-1-methyl-imidazole-2-thiolato-N3,S)-bis{[bis(1-methylimidazol-2-yl) ketone]palladium(II)} nitrate [Pd2(bmik)2(meimt)2](NO3)2 · 4.5 H2O (3). In the cases of 1 and 3 the bridging thiolate ligands show head-to-head orientation. For complex 2 a head-to-tail orientation of the pyrimidine-2-thiolates was found. The metal-metal distances vary from 2.963 Å in complex 3 and 2.915 Å in 1 to the shortest of 2.886 Á in 2. In addition to the X-ray crystallography the three compounds were characterized by 1H-NMR and IR spectroscopy.
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  • 218
    ISSN: 0009-2940
    Keywords: Boranes ; Aminoboranes ; Phosphanyliminoboranes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Contributions to the Chemistry of Boron, 221[1].  -  Kinetic and Thermodynamic Product Control in the Addition of HX Compounds to an Amino Phosphanylimino Borane R2N—B≡N—PR2′The reaction of equimolar amounts of HI with tmp=B≡N—PtBu2 (3) (tmp = 2,2,6,6-tetramethylpiperidino group) in an unpolar solvent yields the phosphonium salt [tmp-B=N—PHtBu2]I (4). No such well-defined reaction was observed with triflic or tetrafluoroboric acid. In contrast, HCl reacts with 3 to produce a mixture of tmp-B(Cl)-NH-PtBu2 (5) and tmp - B(Cl) - N=PHtBu2 (6). On heating or on standing at ambient temperature the unique proton of 5 migrates from the N to the P atom with formation of 6, which, therefore, is thermodynamically more stable than 5.
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  • 219
    ISSN: 0009-2940
    Keywords: (Trifluoromethyl)sulfane- and -disulfanesulfonic acids ; Mercury compounds ; (Trifluoromethyl)sulfanyl-disulfanyl-, and -sulfinylimine ; Arsenic compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Properties of S-(Trifluoromethyl)polysulfanemonosulfonates CF3SxSO2M [x=1, M = OH, NH4O, 1/2 HgO2, (CH3)2N, NH2; x=2, M = NH4O]*Hydrolysis of CF3SNSO with 2 equiv. of H2O provides [NH4][CF3SSO3] (1), which on treatment with chlorine gives CF3SCl and [NH4][ClSO3]. Trifluoromethyl thiosulfates are synthesized from Hg(SCF3)2 and ClSO2M [M = NH4O, (CH3)3SiO (2), (CH3)2N (3), NH2 (4)]. Insertion of SO3 into Hg(SCF3)2 provides Hg[CF3SSO2O]2 (6). Similarly, S-(trifluoromethyl)thiosulfuric acid (5) is obtained from CF3SH and SO3. New preparations for CF3SXNSO (x=1, 2) are described. These compounds are formed either from Hg(NSO)2 or (CH3)3SiNSO and CF3SxCl in good yields. CF3SSNSO (8) reacts with water to give [NH4][CF3SSSO3] (9). A 1:1 adduct (10) is obtained from CF3SNSO and AsF5. A preliminary X-ray structure investigation proved that AsF5 is coordinated to the oxygen atom. Some reactions of [NH4][CF3SSO3] and CF3SSO2OSi(CH3)3 are mentioned.
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  • 220
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 501-506 
    ISSN: 0009-2940
    Keywords: Tripod ligand synthesis ; Tripod iron trisacetonitrile complexes ; Tripod cobalt acetate complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Functionalized Tripod Ligands: Synthesis and Coordination of 1,1,1-Tris[(diphenylphosphanyl)methyl]methaneThe tripod ligand HC(CH2PPh2)3 (4) is easily available from the reaction of 1,3-dichloro-2-(chloromethyl)propane (3) with lithium diphenylphosphide. The ligand 4 itself and two of its coordination compounds, [(HC(CH2PPh2)3)Co(OOCMe)]+-[BPh4]- (5 · BPh4) and [(HC(CH2PPH2)3)Co(OOCMe)]2+ · 2[BF4]- [7 · (BF4)2] have been characterized by X-ray analyses. Coordination of 4 leads to an opening of the CH2—CH—CH2 bond angles (114° in 7 · (BF4)2 and 5 · BPh4 versus 111° in 4). This change in structure is reflected by the unusual low field shift of the methine hydrogen of 7 · (BF4)2 (δ = 3.90) in comparison with the corresponding signal of the free ligand 4 (δ = 1.53).
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  • 221
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 11-14 
    ISSN: 0009-2940
    Keywords: Niobium iodide telluride ; Polytellurides ; Chain compounds, one-dimensional ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The new ternary compound Nb4Te17I4 has been prepared and structurally characterized. It crystallizes in the monoclinic system, space group C2/c with unit-cell parameters a = 16.199(4), b = 8.128(2), c = 27.355(6) Å, β = 110.84(2)°, Z = 4. The structure consists of infinite one-dimensional niobium/tellurium chains running parallel to the crystallographic c direction. The chains are separated by iodine atoms. Short and long metal-metal distances alternate in the sequence of three consecutive short bonds ([d ≈ 3.1 - 3.2 Å) and one long (d = 4.268 Å) metal-metal separation. Each Nb atom is eight-coordinate. The composition of the chain is ∞11[(Nb5+)2(Nb4+)2(Te22-)4(Te32-)3(I-)4].
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  • 222
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 15-21 
    ISSN: 0009-2940
    Keywords: Copper niobium telluride ; Layer compounds ; Low-dimensional compounds ; Electrical properties ; Band structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis, Structure and Electronic Properties of Cu0.69NbTe2Cu0.69NbTe2 is obtained from the elements in a sealed quartz ampoule at 850°C. The structure of Cu0.69NbTe2 is related to the CdI2 type. The Cu atoms are disordered and situated in tetrahedral sites between the NbTe2 layers. The Nb atoms form zig-zag chains extending in one direction within the layers. This deformation of the Nb sublattice from trigonal symmetry is typical for CdI2 derivatives with formal electron counts close to d2 on the early transition metal. The magnetic susceptibility is temperature-independent between 4 K and 300 K (Pauli paramagnetism). Resistivity measurements confirm the metallic behavior of the compound. The crystal structure and the physical properties are in agreement with the results of tight-binding band-structure calculations.
    Additional Material: 7 Ill.
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  • 223
    ISSN: 0009-2940
    Keywords: Organosilicon p-phenylenediamine derivatives ; Wurster's blue ; PE spectroscopy ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Structures of Sterically Overcrowded and Charge-Perturbed Molecules, 38[1].  -  The Different Conformations of N-Trimethylsilyl-Substituted p-Phenylenediamine Derivatives: Investigation of Single Crystals and in the Gas PhaseThe ESR-proven generation of a Wurster's Blue radical anion by one-electron reduction of N,N,N′,N′-tetrakis(trimethylsilyl)-p-phenylenediamine is rationalized by a posterior singlecrystal structure determination of the neutral molecule, which demonstrates inter alia that the bulky [(H3C)3Si]2N substituents are twisted out of the benzene plane by 83°. In contrast, the skeleton of the sterically congested N,N′-bis(trimethylsilyl)-p-phenylenediamine remains almost planar and, accordingly, allows nN/π interaction between the p-type nitrogen electron pairs of the also flattened [(H3C)3Si]HN groups and the benzene π system. These conformational differences are reflected in the gas-phase photoelectron spectra, in which nN/π ionisation bands are split by less than 1 eV or more than 3 eV, respectively. The evidence for analogous structures of the two organosilicon p-phenylenediamine derivatives in solution is confirmed by geometry-optimized AM1 calculations, which readily explain the surprising insertion of an extra electron into an already electron-rich molecule.
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  • 224
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 97-99 
    ISSN: 0009-2940
    Keywords: (Sulfinylthio)phthalimides ; Thiosulfinato complexes ; Platinum complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oxidative addition of N-[(alkyl- and arylsulfinyl)thio]-phthalimides 3a-d to Pt(PPh3)2(C2H4) gives the platinum(II) thiosulfinato complexes cis-Pt[(S-S(O)-R)(Nphth)(PPh3)2] 4a-d; the structure of N-[(benzylsulfinyl)thio]phthalimide (3c) has been characterized by X-ray crystallography.
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  • 225
    ISSN: 0009-2940
    Keywords: Host-guest complexes ; Molecular-dynamics (MD) simulation ; Enantioselective gas chromatography ; Cyclodextrins ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The energies of complexation of methyl (R)/(S)-2-chloropropionate [(R)/(S)-2] with heptakis(3-O-acetyl-2,6-di-O-pentyl)-β-cyclodextrin (1) and the structures of the corresponding complexes were determined by molecular-dynamcis (MD) simulations at 300 and 333 K. The geometry of the complexes, the conformations of complexed and uncomplexed 1 and (R)/(S)-2 and the closest H-H distances between host and guest in the complexes were determined from the trajectories. The results correspond to the experimental findings from enantioselective gas chromatography.
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  • 226
    ISSN: 0009-2940
    Keywords: Triquinacenes ; Indenoindenes ; syn Elimination ; thermal ; Conformational effects ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of tribenzotriquinacene 4 by a stepwise cyclization strategy involving phenyl-substituted diindan intermediates is discussed in detail. Based on the determination of the anti (α) stereochemistry of the previously known phenyldiindanone 8 by standard electron impact mass spectrometry as well as on synthetical evidence (8 → 12 → 14), the conversion of 8 to the syn (β) phenyl-substituted isomer 20 by means of dehydrogenation-rehydrogenation sequences has been achieved. In particular, the preparation of the isomeric diindenones 15 and 16 as key synthetic intermediates by thermal syn elimination of the corresponding phenylsulfinyl and phenylseleninyl ketones 22 and 25 is described and contrasted to a bromination/dehydrobromination approach adopted from a previous report. The synthesis is completed by reduction of 20 to diindanol 27 followed by cyclodehydration, giving 4 in 14-19% overall yield from 8. Non-cyclizing dehydration of 27 and the isomeric diindanol 9 gives the Δ4b,9-diindene 30 as the most stable non-cyclized isomer of 4. The steric effect of the syn- or anti-oriented phenyl substituents on the preferred conformation of the diindan skeleton is deduced from the contrasting vicinal 1H-1H spin coupling observed for the stereoisomers, e.g. the 9-phenyldiindans 28 and 29.
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  • 227
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 201-204 
    ISSN: 0009-2940
    Keywords: Diazo compounds ; Homologation ; Valence isomerization ; Germanium compounds ; Tetrahedranes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Small Rings, 80[1].  -  Tri-tert-butyl(trimethylgermyl)cyclobutadiene and Tri-tert-butyl(trimethylgermyl)tetrahedraneIn the course of our research on silyl-substituted diazo compounds as precursors of cyclobutadienes and tetrahedranes the synthesis of the title compounds 16 and 17 has also been accomplished. Their properties are comparable to those of the silyl-substituted homologous compounds. Tri-tert-butyl(trimethylgermyl)tetrahedrane (17) melts without decomposition at 143°C and thus proves to be as stable as tri-tert-butyl(trimethylsilyl)tetrahedrane. The interconversion of the rectangular forms of tri-tert-butyl(trimethylgermyl)cyclobutadiene (16) proceeds with an activation energy below 4 kcal/mol, which is nearly the same as of tri-tert-butyl(trimethylsilyl)cyclobutadiene.
    Additional Material: 1 Tab.
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  • 228
    ISSN: 0009-2940
    Keywords: Alkenes ; hyperstable ; Hydrogenation ; catalytic ; Hydrocarbons ; concave ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: (1α,6α,7α,8α,12α,17α,18α,19α)-Heptacyclo[17.3.1.18,12.05,23.06,18.07,17.016,24]tetracosa-5(23),16(24)-diene, a Hyperstable AlkeneHydrogenation of the cis-photodimer 1 of acenaphthylene yields the title compound 2, which, though still containing two double bonds, undergoes no further hydrogenation or reaction with bromine for steric reasons. The cyclobutane ring of 2 shows strong steric distortions as revealed by X-ray analysis as well as by force-field and semiempirical MO calculations.
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  • 229
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 261-265 
    ISSN: 0009-2940
    Keywords: Bond activation ; C—H ; C—C ; Iron chemistry ; Reaction mechanisms ; Chelate effects ; Tandem mass spectrometry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: For three α,ω-diphenylalkanes the mechanistic details of the Fe+-mediated activation of C—H and C—C bonds in the gas phase have been elucidated by isotopic labelling experiments. The unimolecular reactions, i.e. dehydrogenation of the alkane chain, formation of ethylene from internal methylene groups, and generation of toluene, proceed largely with high selectivity. Particularly interesting are the results for the dehydrogenation of the Fe+ complex 3-Fe+ of 1,8-diphenyloctane which involves to 93% the internal methylene groups C-4/C-5. In addition, the study of the stereoisotopomers 3c-d provides evidence for the operation of isotopically sensitive branching (“metabolic switching”) in the reaction, and the analysis of the data suggests that the selectivity of the reaction is, most likely, due to a sandwich-type structure.
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  • 230
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 271-274 
    ISSN: 0009-2940
    Keywords: Pig liver esterase ; Enantioselective hydrolysis ; Asymmetrized neopentane ; Reactive chiral building block ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A Novel Chiral Building Block with Neopentane Framework for Synthesis: Chemo-Enzymatic Preparation of (R)-CH3C(CH2OSO2CF3)(CH2Cl)(CH2Br)The pig liver esterase (PLE) catalysed hydrolysis of the prochiral malonic ester (BzlOCH2)(Me)C(COOMe)2 (1) leads to its chiral monoester 2 in selectivities up to 81% ee. Compound 2 is an ideal entry point for the enantioselective synthesis of 1,1′,1″-substituted neopentanes CH3C(CH2X)-(CH2Y)(CH2Z) with three different leaving groups, X, Y, and Z. CH3C(CH2OSO2CF3)(CH2Br)(CH2Cl) (8) is a versatile reactive building block for the asymmetric synthesis of compounds containing the neopentane-C5 skeleton.
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  • 231
    ISSN: 0009-2940
    Keywords: Heterobimetallic complexes ; Iron complexes ; Platinum complexes ; Silyl complexes ; Phosphido bridges ; Hydrido complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Transition Metal Silyl Complexes, 48[1]. - Synthesis of the New Heterobimetallic Dinuclear Silyl Complexes (OC)3(R3Si)-Fe(μ-PR′R″)Pt(1,5-COD)(Fe-Pt), Phosphane Exchange Reactions of (OC)3(R3Si)Fe(μ-PR′R″)Pt(PPh3)2(Fe-Pt), and Preparation of the Dihydrido complexes [(OC)3Fe(μ-PPh2)(μ-H)2Pt(PR3)2][BF4](Fe-Pt)The dinuclear, silyl-substituted complexes (OC)3(R3Si)Fe(μ-PR′r″)Pt(1,5-COD) (1) [μ-PR′R″ = PPh2, PCY2, PHPh; SiR3 = SiPh3, Si(OMe)3] were prepared in high yields by the oxidative addition of the hydrido complexes (OC)3(PHR′R″)Fe(H)-SiR3 to Pt(1,5-COD)2. Upon reaction of (OC)3(R3Si)Fe(μ-PR′R″)Pt(PPh3)2 [μ-PR′R″ = PPh2, PHCy; SiR3 = SiPh3, SiPh2Me, SiPhMeCl, Si(OMe)3] with two equivalents of PR‴3 (PMe3, PBu3, PEt3) or with one equivalent of chelating di-phosphanes (vdpp, dppe, dppm) both PPh3 ligands are displaced, and (OC)3(R3Si)Fe(μ-PR′R″)Pt(PR‴3)2 or (OC)3(R3Si)-Fe(μ-PR′R″)Pt[(PPh2)2X] (X = C=CH2, C2H4, CH2) are formed, respectively. When one equivalent of PMe3 is used, only the PPh3 ligand trans to the μ-PPh2 bridge is substituted, and (OC)3(Ph3Si)Fe(μ-PPh2)Pt(PPh3)(PMe3 is formed. The 1,5-COD ligand in 1 is displaced by P(OR)3 to give (OC)3-(Ph3Si)Fe(μ-PPh2)Pt[P(OR)3]2 (R = Me, Ph). The complexes (OC)3(Ph3Si)Fe(μ-PPh2)Pt(PMe3)2and (OC)3(Ph3Si)Fe(μ-PPh2)Pt[(PPh2)2C=CH2] were characterized by X-ray structure analysis. The short Fe-Si distances [233.0(2) and 235.6(3) pm] and the infrared v(CO) absorptions indicate that the Fe-Pt bonds are quite polar. Protonation of (OC)3(Me2-PhSi)Fe(μPPh2)Pt(PPh3)2 with CF3COOH gives the hydrido-bridged complex [(OC)3(Me2PhSi)Fe(μ-PPh2)(μ-H)Pt-(PPh3)2][O2CCF3]. Upon addition of an excess of HBF4 · Et2O to (OC)3(R3Si)Fe(μ-PPh2)Pt(PPh3)2 (R = Ph, OMe), (OC)3-Si)Fe(μ-PPh2)Pt[Pt[P(OMe)3]2 or (OC)3(Ph2MeSi)Fe(μ-PPh2)-Pt(dppe) R3SiF is split, and the corresponding μ-dihydrido complexes [(OC)3Fe(μ-PPh2)(μ-H)2Pt(PR3)2][BF4] are obtained.
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  • 232
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 343-346 
    ISSN: 0009-2940
    Keywords: Azole-borane adducts ; Azaboles ; Imidazabole ; X-ray analysis ; NMR, multinuclear ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Elimination of H2 from the imidazole - borane adduct 1 leads to a mixture of the imidazaboles 2 and 2′. The symmetrical isomer 2 (two H2BNC fragments) is isolated in pure state and characterized by an X-ray structure analysis (monoclinic, space group P21). 2-(Trimethylstannyl)thiazole (3a) and 1-methyl-5-(trimethylstannyl)-1,2,4-triazole (3b) react with triethylborane to form adducts 4 from which, in the presence of an excess of Et3B, tetraalkyltin is elimated to give the thiazabole 5a and the triazabole 5b, respectively. Multinuclear 1H-, 11B-, 13C-, 14N-, and 119Sn-NMR spectroscopy serve for following the reactions (compounds 3 to 5) and to characterize all final products.
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  • 233
    ISSN: 0009-2940
    Keywords: Tin cations ; triorgano ; Coordination ; s̰ and π ; 1,1-Organoboration ; 1-Alkynyltin compounds ; functionally substituted ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Di-1-alkynyltin compounds 1 of the type Me2Sn(C≡CUL)2 [LU = 2-pyridyl (a), Me2NCH2 (b), MeOCH2 (c), MeOCH=CH (d), EtSCH2 (e)] were prepared and the 1,1-organoboration of 1 with triethyl- (2a) and triisopropylborane (2b) has been studied. The first detectable intermediates were in all cases zwitterionic compounds 3 (from Et3B) and 4 (from iPr3B) with a cationic triorganotin fragment, stabilized by coordinative s̰ L—Sn bonds and by side-on coordination to the C≡C bond of an alkynylborate moiety. The nature of this stabilization has been established by three X-ray analyses (3b, 4b, and 4d) in the solid state and by multinuclear NMR (1H-, 11B-, 13C-, 15N-, 119Sn NMR) in solution. The comparison of the molecular structure of 3b, 4b, and 4d with that of intermediates without functional groups shows that the distance of the tin atom to the C≡C bond is elongated. However, the planar arrangement of all relevant atoms proves that the side-on coordination of the tin atom to the C≡C bond is still present. These intermediates 3 and 4 rearrange to stannoles 5, 6 and/or to 1-stanna-4-bora-2,5-cyclohexadienes 9, 10. In the case of 3b and 3e, 119Sn NMR indicates that dialkenyltin compounds 7b and 7e are also formed as minor products. In the case of 3e, the 3-stannolene 8e is one of the final products. In the stannoles 5 and 6 a coordinative L—B bond is evident, and there is NMR spectroscopic evidence of a weak coordinative L - Sn bond.
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  • 234
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 393-400 
    ISSN: 0009-2940
    Keywords: Cyclovoltammetry ; Charge-transfer complexes ; HOMO energy ; Naphthols ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Measurement of the Donor Strength of Substituted 1-NaphtholsThe oxidation potential of various substituted naphthols is available by cyclovoltammetry. The donor strength of substituents on the oxidation potential may be explained on the base of substituent increments. When correlating the oxidation potential with the transition energy of charge transfer complexes with TCNE, 1-naphthols with 8-alkoxy substituents and naphthols without oxygen in position 8 are giving different correlation curves. The experimental values correlate well with semiempirically calculated HOMO energies. Our measurements allow to predict the oxidation potentials of hitherto unknown substituted 1-naphthols with high probality. Thus, it may be possible to synthesize 1-naphthols with a defined oxidation potential.
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  • 235
    ISSN: 0009-2940
    Keywords: Fenestranes ; Polyquinanes ; Centropolyindans ; Polycyclic compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and spectroscopic characterization of several benzoanellated [5.5.5]-, [5.5.5.6]-, and [5.5.5.5]fenestranes, including the parent difuso-centrotriindan 7, the parent tetrafuso-centrotetraindan 8 (“fenestrindan”) as well as the tribenzo[5.5.5.6]- and tribenzo[5.5.5.5]fenestranes 27 and 35, are described and discussed in full experimental detail. The highly efficient twofold cyclodehydration of 2,2-dibenzyl-1,3-indandiol 15 and the related spiro-condensed 1,3-indandiols 23 and 29 is the keystep of the synthetic strategy. The new synthetic variant involving the one-pot cyclodehydration/deketalization of the dispiro-ketal diol 29 is particularly convenient. In the case of 7, an alternative Lewis acid-catalyzed double cyclization has been developed. Stereochemical aspects of the 1,3-indandiols and the key tribenzo[5.5.5.6]fenestranes 24 and 25 are discussed in detail.
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  • 236
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 437-444 
    ISSN: 0009-2940
    Keywords: Reductive coupling ; Oligo(9,10-anthrylene)s, derivatization of, cyclization of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A homologous series of oligo(9,10-anthrylene)s up to the heptamer have been synthesized by reductive coupling of quinones with lithioanthrylenes, followed by reductive aromatization of the intermediate hydroxy species. The method used allows the introduction of different alkyl substituents, which ensure sufficient solubility of the newly synthesized anthrylene systems in common organic solvents. The solid-state conformations of trimers 4 and 5 have been established by X-ray structure analysis; UV/Vis-spectroscopic investigations in solution reveal the anthracene moieties in 9,10-anthrylenes to exist as electronically independent electrophores. The trianthrylenes can be subjected to electrophilic substitution which regioselectively provides e.g. 10-bromo- and 10,10″-dibromo derivatives. These bromides can easily be converted into the corresponding cyano compounds. Under the influence of potassium hydroxide in quinoline the trimer 5 partially cyclizes to helianthrene compounds.
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  • 237
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. A19 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 238
    ISSN: 0009-2940
    Keywords: Copper(II) complexes, dinuclear ; Schiff bases, macrocyclic ; Redox properties ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexes with Macrocyclic Ligands, I. - Dinuclear Copper(II) Complexes with a Totally π-Conjugated Macrocycle of Schiff Base Type: Syntheses, Structures, Electro-, and Magnetochemical PropertiesThe dinuclear copper(II) complexes 6, 7, and 8 of three novel macrocyclic ligands were synthesized by the Schiff base condensation of 2 equiv. of 1,2-phenylenediamine and 2,6-diformylphenol in the presence of 2 equiv. of copper(II) perchlorate and were characterized by X-ray structure analyses, electrochemical investigations (DCV), and variable-temperature magnetic susceptibility measurements. Complex 6 exists in two different solvated crystalline forms. The Copper(II) ions in all three complexes are octahedrally coordinated with long axial distances to solvent molecules or perchlorate ions. The copper ions in 6 (in solvate a) are only five-coordinate and square-pyramidal. The CuIICuII complexes were reduced in successive, quasi-reversible, one-electron steps. The antiferromagnetic exchange interactions were determined. Upon dissolution in acetonitrile complex 8 decomposed to form [Cu(MeCN)4]+ClO-4 and the benzimidazolium percholorate 9 (X-ray structure determination).
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  • 239
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 489-500 
    ISSN: 0009-2940
    Keywords: Alkenes ; Nickel complexes ; Stannenes ; Metal-metal bonds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: {Bis[bis(trimethylsilyl)methyl]stannio(II)}bis(η2-ethene)nickel(0) and Related Compounds, Part IIThe coordinatively unsaturated (16e) (ethene)nickel(0) stannylene complex (C2H4)2Ni=Sn{CH(SiMe3)2}2 (1) reacts with 1,6-heptadiene with preservation of the Ni=Sn bond to yield quantitatively the 1,6-diene derivative (η2,η2-C7H12)Ni=Sn-{CH(SiMe3)2}2 (2). The alkene ligands of both 1 and 2 are readily displaceable. Compounds 1 and 2 react with butadiene at -50°C by a 4-e oxidation of the metal-metal pair Ni(0)/Sn(II) to Ni(II)/Sn(IV) and concomitant reduction of two butadiene molecules to butenediyl moieties to afford stereo-selectively the 16-e complex Ni-cis-{η3(Ni),η1(Sn)-anti-C3H4CH2}2Sn{CH(SiMe3)2}2 (3). Similarly, the reaction of 1 or 2 with isoprene yields regio- and stereoselectively the derivative Ni-cis-{η3(Ni,η1(Sn)-anti-C3(3-Me)H3CH2}2Sn{CH-(SiMe3)2}2 (4). These reactions imply the cleavage of one formal Ni—Sn bond and the formation of two new Sn—C bonds. Upon reaction of 3 with PMe3 the configuration of the allyl system changes and, again fully stereoselectively, the 18-e addition compound (Me3P)Ni-cis-{η3(Ni),η1(Sn)-syn-C3H4-CH2}2Sn{CH(SiMe3)2}2 (5) is formed. When 5 is treated with BPh3, the phosphane ligand is trapped and, kinetically controlled, Ni-cis-{η3(Ni),η1(Sn)-syn-C3H4CH2}2Sn{CH(SiMe3)2}2 (6) is obtained as a stereoisomer of 3. At 40°C 6 slowly rearranges into the thermodynamically stable stereoisomer Ni-trans-{η3(Ni),η1(Sn)-syn-C3H4CH2}2Sn{CH(SiMe3)2}2 (7). Mild protolysis of 3 with pyridine hydrochloride or hydrobromide affords region and stereoselectively (Me3Si)2CH}2(X)SnNi-(η3-1-MeC3H4)(NC5H5) (X = C1, 8a; Br, 8b). In the course of this protonation reaction one butadiene molecule is eliminated, accompanied by a 2-e reduction of the metal-metal pair Ni(II)/Sn(IV) to Ni(II)/Sn(II) and, at the expense of two Sn—C bonds, reformation of a Ni—Sn bond. All compounds are isolated in high yield and fully characterized by 1H-, 13C-, and 31P-NMR spectroscopy.
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 533-539 
    ISSN: 0009-2940
    Keywords: Bissulfenyl chlorides ; fluoro substituted ; 1,3-Dithioles ; 1,3,2-Dithiazoles ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Halogen-Carbon-Sulfur Compounds: Syntheses with 1,1,1,4,4,4-Hexafluoro-2-butene-2,3-bissulfenyl ChlorideThe bifunctional bissulfenyl chloride 3 is obtained by chlorination of the dithiete 1 or tetrathiocine 2. By excessive chlorination the saturated bissulfenyl chloride 4 is formed. 3 reacts with primary amines to yield the 1,3,2-dithiazoles 5a-e, whereas by reactions with active methylene compounds like ketones or β-dicarbonyls the compounds 7-14 are obtained with HCl elimination. 13 as well as 14 are converted into the carboxylic acid 15 from which the 1,3-dithiole 17 is obtained by decarboxylation. 3 reacts with disulfene to form tetrakis-(trifluoromethyl)tetrathiafulvalene as well as 4,4′,5,5′-tetrakis(trifluoromethyl)-2,2′-spirobi[1,3-dithiole] (18), whose crystal structure has been determined.
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  • 241
    ISSN: 0009-2940
    Keywords: Hydrogen transfer ; Molecule-induced radical formation ; Reduction of C—F bond ; 1-Adamantylfluorodiphenylmethane ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1-Adamantylfluorodiphenylmethane (2) was reduced to 1-adamantyldiphenylmethane (3) when heated with 9,10-dihydroanthracene to 330°C. From the second-order kinetics, the activation parameters (ΔH
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  • 242
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    Berichte der deutschen chemischen Gesellschaft 127 (1994) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 243
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 611-613 
    ISSN: 0009-2940
    Keywords: 2,3-Diboratetralin,2,3-bis(dimethylamino)- ; 2,3-Diboranaphthalenediide,2,3-bis(dimethylamino)- ; 2,5-Benzodiborocine,2,5-bis(dimethylamino)-3,4-diethyl-1,2,5,6-tetrahydro- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis, Deprotonation, and Ring Expansion of a 2,3-DiboratetralinHerrn Prof. Dr. Helmut Werner zum 60. Geburtstag gewidmet.Reaction of K2[1,2-C6H4(CH2)2] with [Cl(Me2N)B]2 leads to 2,3-bis(dimethylamino)-2,3-diboratetralin (4a) in 58% yield. Deprotonation of 4a with lithium 2,2,6,6-tetramethylpiperi-dide yields the crystalline dilithium salt 6a. Insertion of 3-hexyne into the B—B bond of 4a results in the formation of 2,5-bis(dimethylamino)-3,4-diethyl-1,2,5,6-tetrahydro-2,5-benzodiborocine (7a) in 38% yield. The constitutions of 4a, 6a, and 7a were derived from 1H-, 11B-, 13C-NMR, and MS data and proven for 6a and 7a by X-ray,structure analyses.
    Additional Material: 2 Ill.
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  • 244
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 631-637 
    ISSN: 0009-2940
    Keywords: N-Isocyanodialkylamines ; N-Isocyanide metal complexes ; Homoleptic complexes ; Stabilization by coordination ; N—N Bond cleavage ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal Complexes of Functional Isocyanides, XXIII[1]. - N-Isocyanodialkylamine Complexes of Boron, Rhodium, Palladium, Platinum, and CopperThe N-isocyanodialkylamines CNNEt2, CNNiPr2, and CNNCH(Me)(CH2)3CHMe (1a-c) react with triphenylboron, various transition metal halides, and mono- and dinuclear chloro complexes by addition, substitution, bridge cleavage and reduction to give the complexes Ph3BCNNR2 (2b, c), [MX2(CNNR2)2] (M = Pd, Pt; X = Cl, Br, I) (3-7), [M(Cl)-(CNNR2)(PPh3)2]BF4 (8, 9), cis- and trans-[PtCl2(CNNR2)-(PR′3)] (R′ = Et, Ph) (10-12), [Rh(CNNR2)4]Cll (15b, c) and [Cu(CNNR2)4]ClO4 (16b, c). The complexes [PdX2(CN—NR2)(PPh3)] (X = Cl, Br) (13c, 14c) have been obtained by substitution of an N-isocyanide ligand in 3c and 4c, respectively, with PPh3. The structural assignments are made on the basis of IR, NMR (1H, 13C, 31P, 15N) and mass spectrometry as well as of an X-ray structure analysis of [PdI2(CNNiPr2)2] (5b).
    Additional Material: 1 Ill.
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  • 245
    ISSN: 0009-2940
    Keywords: Ethaneselenol, pentafluoro-, IR, Raman, NMR, electron diffraction ; ab initio Calculation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactive E=C(p-p)π Systems, XXXVII[1]. - Pentafluoroethaneselenol: Synthesis, Spectra, and Gas-Phase StructureHerrn Professor Wolfgang Sawodny zum 60. Geburtstag gewidmet.Pentafluoroethaneselenol HSeC2F5 (1) and its deuterated analogue DSeC2F5 (2) are obtained in moderate yields by cleavage of the diselane (SeC2F5)2 with Me3SnH and Me3SnD, respectively. Complete characterization of the labile compounds was accomplished by spectroscopic investigations (IR, Raman, MS; 1H, 13C, 19F, 77Se NMR). The molecular structure was determined by electron diffraction in the gas phase together with ab initio calculations.
    Additional Material: 3 Ill.
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  • 246
    ISSN: 0009-2940
    Keywords: Organoiron compounds ; Iron catalysts ; Ketone synthesis ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alkyliron and Alkylcobalt Reagents, IX[1].  -  Rearrangement of Aliphatic Terminal Epoxides to Methyl Ketones by Iron Alkyl Reagents instead of Co2(CO)8 or Noble Metal CatalystsThe highly selective rearrangement of aliphatic terminal epoxides to methyl ketones, hitherto possible only with Co2(CO)8 or noble metal catalysts, occurs smoothly with Me4-FeLi2, Me3FeLi, or the catalytic systems [RLi + 2.5 mol% FeCl3] (R = Me, Bu). This was demonstrated by the rearrangement of 1-decene oxide (1) to 2-decanone (2) (yield 80-81%; Table 1) and 6-bromo-1-hexene oxide (5) to 6-bromo-2-hexanone (6) (yield 78%, Me4FeLi2 applied only). The competition reaction of Me4FeLi2 with 1 and 2-octanone (8) (mole ratio 0.5:1:1) led to 87% 2-methyl-2-octanol (9) and not to the rearrangement 1 → 2. This indicates that Me4FeLi2 - in contrast to the opposite behavior of organo cuprates - reacts faster with ketones than with the aliphatic terminal epoxides. By treatment of 1 with methyl derivatives of MnII, CoII, and NiII or with Bu4FeLi2 (Table 2) other products (3, 4) besides 2 were formed. The rearrangement of 1 with Me4FeLi2 is assumed to start with an oxidative addition and yields 2 as its Li or Fe enolate (trapped with acetanhydride to give 64% of 20) after reductive elimination of CH4. The catalytic rearrangement of 1 with [MeLi + 0.25 mol% FeCl3] very probably occurs in an analogous manner with an super-ate complex Me4FeLi2(MeLi)n as the active species and the Li enolate of 2 as end product (Scheme 4). The aromatic terminal epoxides styrene oxide and α-methylstyrene oxide give various products in the reaction with Me4FeLi2 or Me3FeLi, including the deoxygenation products styrene and α-methylstyrene. These products are exclusively formed on treatment of the epoxides with Me4MnLi2. (Prepared, hitherto in the literature not described compounds: 7 and 10-15.)
    Additional Material: 3 Tab.
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  • 247
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 691-696 
    ISSN: 0009-2940
    Keywords: Molecule-induced radical formation, kinetics of ; Catalysis ; ESR spectroscopy ; Radical clock ; Isokinetic relationship ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bimolecular Formation of Radicals by H-Transfer, 7[1].  -  Bimolecular Formation of Radicals via H-Transfer with Catalysis by 7H-Benz[de]anthraceneThe transfer hydrogenation of α-methylstyrene (2) by 9,10-dihydroanthracene (1) (DHA) with 7H-benz[de]anthracene (8) as a catalyst proceeds already at 210-260°C. Isotopic labeling, ESR spectroscopy, radical clock experiments, solvents effects, and thermochemical calculations support the postulated stepwise radical mechanism induced by bimolecular formation of radicals.
    Additional Material: 4 Ill.
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  • 248
    ISSN: 0009-2940
    Keywords: [2-(Acylamino)ethenyl]carbene complexes ; Aminocarbene complexes of chromium and tungsten ; Ketene imines, 2-(acylamino)ethenyl ; Pyrroles, synthesis by ring-closing metathesis ; 1,4-Diaminonaphthalenes, synthesis by electrocyclization ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic Syntheses via Transition Metal Complexes, 69[1].  -  2-(Acylamino)ethenyl Ketene Imines from [2-(Acylamino)ethenyl]carbene Complexes and their Ring-Closing Metathesis to Pyrroles or Electrocyclization to 1,4-DiaminonaphthalenesHerrn Prof. Helmut Werner zum 60. Geburtstag gewidmet.[2-(Acylamino)ethenyl]carbene complexes LnM = C(OEt) —CH=CPh—[N(COR)Ph] 5 [LnM = (CO)5Cr, (CO)5W; R = C6H5, pMeOC6H4, pNO2C6H4, OtBu] are obtained by N-acylation of [2-(amino)ethenyl]carbene complexes LnM=C (OEt)-CH=CPh(NHPh) (Z)-3 in 72-90% chemical yields with high stereoselectivity. The reaction of (Z) - or (E)-5 with two equivalents of isocyanides RNC 6 (R = cC6H11, tBu) at 20°C gives the isocyanide complexes LnM(RNC) 9 and the [2-(acylamino)ethenyl]ketene imines RN=C=C(OEt)—CH = CPh[N(COR)Ph] 8 (〉95% yields) with configurational retention at the C=C(N) bond. Thermolysis of (Z)-8 (20-80°C) provides an efficient route to pyrroles 11 (90-95%) by a ring-closing metathesis with elimination of isocyanates 10, while the thermolysis of (E)-8, e.g. (E)-8g, at 20°C leads to the formation of 1,4-diaminonaphthalenes, e.g. 12g (〉95% yield), by an electrocyclic ring closure.
    Additional Material: 1 Ill.
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  • 249
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 759-765 
    ISSN: 0009-2940
    Keywords: Chirality ; Circular dichroism ; Conformational mobility ; Cyclophanes ; [n]Phanes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Deformed Chiral [n]MetacyclophanesThe new dithiametacyclophane 3c and the thiaazametacyclophanes 6a, b are chiral, but do not contain chirality centres. They are obtained by cyclization of 1,3-propanedithiol (2), or of the thiaza precursors 5a, b, with the bis(bromomethyl) compounds 1, 4a, b. The dynamic behaviour of the aliphatic chains in 3c, and 6a, b (flipping/rotation) have been studied by dynamic NMR. X-ray analyses of 3c and 6a document the out-of-plane deformation of the boat-shaped benzene ring. The circular dichroism of enantiomer-enriched 3c is reported.
    Additional Material: 2 Ill.
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  • 250
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 783-785 
    ISSN: 0009-2940
    Keywords: Tellurides, organo ; Substitution, aromatic ; Tellurium-copper couple ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Te-Cu couple generated in situ by the reaction of disodium telluride with copper(I) iodide in dry N-methyl-2-pyrrolidone has been found to be a convenient telluration reagent for some activated iodoarenes 1. Using this reagent system, we have prepared by a one-pot synthesis in satisfactory yields several bis(nitroaryl) tellurides 4, which are otherwise laborious to obtain.
    Additional Material: 1 Tab.
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  • 251
    ISSN: 0009-2940
    Keywords: [2-(Amino)ethenyl]carbene complexes ; 3-Amino-1,2-propadienylidene complexes ; (2,3,4,6-Tetra-O-pivaloyl-β-D-galactopyranosylamine, carbene complexes of ; Ketene imines ; Isocyanides ; Pyrroles ; Alkynylcarbene complexes of chromium and tungsten ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic Syntheses via Transition Metal Complexes, 70[1].  -  [2-(Galactopyranosylamino)ethenyl]carbene and 3-(Galactopyranosylamino)-1,2-propadienylidene Complexes on 3-Addition of 2,3,4,6-Tetra-O-pivaloyl-β-D-galactopyranosylamine to Alkynylcarbene Complexes (M = Cr, W).  -  Atropisomeric Galactopyranosyl Pyrroles by Reaction of [2-(Galactopyranosyl-amino)ethenyl]carbene Complexes with IsocyanidesEnantiomeric pure (2-aminoethenyl)carbene complexes LnM=C(OEt)—CH=C(Ph)NHR* (Z)-3 and 3-amino-1,2-propadienylidene complexes LnM=C=C=C(Ph)NHR* 4 [R* = 2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl] are obtained by the addition of galactopyranosylamine R*-NH2 2 to the corresponding alkynylcarbene complexes LnM=C(OEt)—C≡CPh 1 [LnM = (CO)5Cr, (CO)5W]. Treatment of (Z)-3 with two equivalents of tert-butyl isocyanide (5) affords isocyanide complexes 6 and ketene imines 7. The latter cyclize spontaneously to give galactopyranosylpyrroles 8 which form stable atropisomers 8A and 8B.
    Additional Material: 3 Tab.
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  • 252
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 743-757 
    ISSN: 0009-2940
    Keywords: Bond formation ; C—C / Host-Guest complexation ; Metacyclophanes ; Conformation, syn, anti ; Hagihara coupling ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Molecular Tweezers from Cyclophane Building BlocksMolecular tweezer compounds 1-6 with convergent carboxyl groups are prepared from suitable functionalized [2.2]-and dithia[3.3]metacyclophane building blocks by using several multistep strategies. The C—C coupling of two cyclophanes according to the Hagihara method leads to alkynespacered double cyclophanes. These new preorganized, acyclic host compounds of the cyclophane-type react as molecular tweezers and can selectively “grasp” guest molecules and bind them strongly. X-ray analyses underline the syn conformations of the dithia[3.3]- and the anti conformation of the [2.2]metacyclophanes.
    Additional Material: 10 Ill.
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  • 253
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. A41 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 254
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 797-804 
    ISSN: 0009-2940
    Keywords: Heteronuclear complexes ; Ligand [(en)2MIII(OH)2]+ (M = Cr, Co) ; Complexes of third group elements ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexes of Third Group Elements with [(en)2MIII(OH)2] Ligands (M = Cr, Co)Heteronuclear complexes are formed on reaction of cis-[(en)2-MIII(OH)(H2O)]2+ (M = Cr, Co; en = ethylenediamine) with A1III, GaIII, InIII, and T1III in aqueous solution. The following salts with tetranuclear cations have been isolated: [A1{(OH)2-Cr(en)2}3](S2O6)3 · 13 H2O (1), [A1{(OH)2Co(en)2}3](S2O6)3 · 5 H2O (2), [Ga{(OH)2Co(en)2}3](S2O6)3 · 5 H2O (3), [In{(OH)2-Cr(en)2}3](S2O6)3 · 6 H2O (5), and [In{(OH)2Co(en)2}3]-(ClO4)4Cl2 · 4 H2O (6). Furthermore, the dinuclear neutral complexes [InCl4{(OH)2Cr(en)2}] (4) and [TlCl4{(OH)2-Cr(en)2}] · 0.5 H2O (7) are prepared. X-ray analyses confirm that in all cases the [(en)2MIII(OH)2] groups act as bidentate ligands in the hydroxo-bridged heterometallic complexes.
    Additional Material: 7 Ill.
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  • 255
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    Keywords: Chromium tricarbonyl(η6-1,3,5-triphenyl-2,4,6-trimesityl-1,3,5,2,4,6-triphosphatrnane)- ; 1,3,5,2,4,6-Triphosphatriborinane ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation of tricarbonyl(η6-1,3,5-triphenyl-2,4,6-trimesityl-1,3,5,2,4,6-triphosphatriane)chromium (4) is reported. Its X-ray structure reveals an orientation of the Cr(CO)3 moiety with respect to the almost planar B3P3 ring typical of an arene metal tricarbonyl complex.
    Additional Material: 2 Ill.
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  • 256
    ISSN: 0009-2940
    Keywords: Lithium compounds ; Hydrazines ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dilithium N,N′-Bis(trimethylsilyl)hydrazide and a Hydrolysis Product: Side-On- and End-On-Coordinated Li Cations to N2-2 and O2-2N,N′-Bis(trimethylsilyl)hydrazine is converted into the dilithium derivative [(Me3Si)2N2Li2] · 2 thf (1) by nBuLi. Compound 1 forms a tetramer which lies on a crystallographic inversion centre. The Li+ ions are found to be end-on to the N—N units and also coordinated by thf, but three Li+ ions are also positioned symmetrically above the N—N bonds. The hydrolysis of 1 in air leads to the formation of [(Me3SiOLi)4 · Li2O2 · LiN(SiMe3)2] · 2 thf (2) which contains four oxide and one peroxide ions. The O2-2 unit is side-on-coordinated by three Li+.
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  • 257
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 887-892 
    ISSN: 0009-2940
    Keywords: Configuration, absolute ; Alkanols, chiral ; Acetals ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chiral Lactols, XI. - A Method for the Determination of the Absolute Configuration of Chiral AlkanolsChiral secondary alcohols which are protected with the enantiomerically pure lactol 1 or 2 show significant differences in 13C-chemical shifts around the glycosidic linkage. An easy method for determination of the absolute configuration of secondary alcohols based on this fact is described.
    Additional Material: 3 Tab.
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  • 258
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 897-903 
    ISSN: 0009-2940
    Keywords: Dendrimers ; Supramolecular chemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dendrimers and Dendrimer Building Blocks with Trisubstituted Benzene and “Hexacyclene” as Core UnitsThe preparation of new dendritic compounds containing 1,3,5-substituted aromatic units or “hexacyclene” is described. Bulky dendrimers are obtained in few generations starting with polyfunctional core units like 1, 4, 5, 12, and hexacyclene (21). The dendrimers were synthesized by using both the divergent method (for 7) and the convergent method (for 13 and 22). 22 is the first dendrimer containing a crown unit as core.
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  • 259
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 941-946 
    ISSN: 0009-2940
    Keywords: Epoxidation ; Benzofuran ; Benzofuran epoxide ; Quinone methide ; Benzofuran-2-one ; 2,4-Cyclohexadien-1-one, spiroepoxide ; cis-Ene dione ; Perester, β-hydroxy- ; 1,3-Benzodioxole ; Keto enol ester ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oxidation of the benzofurans 1a-f (tetrahydrobenzofurans 1g, h) with excess m-CPBA is reported. The in situ generated, highly reactive benzofuran epoxides 2a-f and their quinone methides 3a-f (cis-ene diones 3g, h) afford the labile tautomeric peroxy esters 5 and 5′ by nucleophilic addition of the peroxy acid. On elimination of m-chlorobenzoic acid, the peroxy esters 5/5′ of the benzofuran derivatives 1a-f rearrange thermally to the keto esters 6 by C—C cleavage or to the spiro epoxides 7 by C—O cleavage. The latter undergo thermal isomerization to the 1,3-benzodioxoles 8 and Diels-Alder cycloaddition to the corresponding dimers 9. Independently, the keto esters 6 and the 1,3-dioxoles 8 were synthesized by thermolysis of the dioxetanes 11. The tautomeric m-CPBA adducts 5/5′ of the persistent ene diones 3g, h, derived from the tetrahydrobenzofuran derivatives 1g, h, rearrange as well to the spiro epoxides 7g, h. In contrast to the benzofuran derivatives 6a-f, the keto enol ester 6h suffers Baeyer-Villiger rearrangement with another molecule of m-CPBA to form the ene diester 10h.
    Additional Material: 1 Tab.
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  • 260
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    Keywords: Bicyclo[3.3.0]octane, derivatives of ; Semibullvalene ; Tricyclo[3.3.0.02-8]octa-3,6-diene ; Cyclooctatetraenes, substituted ; Cyanohydrins, O-(trimethylsilyl)- ; Hydrogen fluoride  -  phosphorus oxychloride  -  pyridine, elimination of trimethylsilanol by ; Phenyl cuprate reagent, conjugate addition of ; Phase-transfer catalysis ; Chlorination by hexachloroethane  -  sodium hydroxide ; Cyclization by dehydrochlorination ; Endoperoxides by triplet oxygen ; 2 H-Pyran, derivative of ; Thermochromism ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Addition of trimethylsilyl cyanide to the diphenylbicyclo[3.3.0]octanedione 8c is catalyzed by the potassium cyanide/18-crown-6 complex and produces a mixture of the diastereomeric bis[O-(trimethylsilyl)cyanohydrins] endo- and exo-10c (3:2). The hydrogen fluoride - pyridine complex in phosphorus oxychloride as solvent and, subsequently, an excess of pyridine convert the mixture of diastereomers 10c into the unsaturated y,y′-diphenyldinitrile 11. This is converted into the red semibullvalene 4 in a single step by treatment with hexachloroethane and concentrated aqueous sodium hydroxide in the presence of tetrabutylammonium hydroxide as phase-transfer catalyst  -  Above 30°C, 4 isomerizes in solution to a mixture of the cyclooctatetraenes 12 and 13. While the red crystals of 4 are stable in the atmosphere, in the dark affording the endoperoxide 16 and the yellow 2H-pyran derivative 17 (7:1) which result from parallel reactions. Only at temperatures as high s 110°C, 16 slowly rearranges to 17 which reacts further to yield well-defined but still unknown products. The simultaneous formation of 16 and 17 at low temperatures is interpreted in terms of endo and exo attack, respectively, of triplet oxygen at the benzylic carbon atoms of the semibullvalene 4 or the isomeric bicyclic diradical 21.  -  The structures of the new compounds are based on spectroscopic evidence and X-ray diffraction analyses of 4, endo-10c, 11, 16, and 17. The semibullvalene 4 exists as a pair of rapidly rearranging degenerate valence tautomers in solution and in the crystal as well. In the solid state, 4 exhibits apparent C2 symmetry and equal atomic distances C2-C8 and C4-C6 (201.9 pm). Because true degeneracy is highly unlikely in the crystal, the equal distribution of two non-equivalent valence tautomers at room termperature results from a fortuitous cancelling of the ΔH° and TΔS° terms governing the equilibrium.  -  The red colour of 4 in the crystal and in solution is due to a maximum at 444 nm which disappears on cooling. Thus, 4 not only belongs to the family of thermochromic semibullvalenes and barbaralanes devoid of a long wavelength chromophor like 1, 6 and 14, but also shows the most intensive maximum at the longest wavelength observed so far.
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    Berichte der deutschen chemischen Gesellschaft 127 (1994) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 262
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 985-990 
    ISSN: 0009-2940
    Keywords: Silyl triflates ; Polysiloxanes ; Polycarbosilanes ; Polysilylenealkynes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bis(trifluoromethylsulfonyloxy)organosilicon Compounds as Synthetic Materials for New Silicon PolymersThe new polycarbosilanes, polysiloxanes, and polysilylenealkynes 1c-6c were obtained by condensation of electrophilic α,ω-bis(trifluoromethylsulfonyloxy)organosilicon compounds 1b-6b with nucleophiles such as organolithium and organomagnesium compounds. The required silyl triflate derivatives 1b-6b have been prepared by reaction of the corresponding amino-, allyl-, or phenylsilanes 1a-6a with trifluoromethanesulfonic acid.
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  • 263
    ISSN: 0009-2940
    Keywords: Copper(II) complexes ; Mangan(II) complexes ; trinuclear ; Schiff bases ; macrocyclic ; Redox properties ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexes with Macrocyclic Ligands, II.  -  Synthesis, Structure and Electrochemical Properties of a Macrocyclic Cu2IIMnII Complex of Schiff Base TypeA novel trinuclear Cu2Mn complex 4 of a macrocyclic Schiff base ligand obtained by condensation of 5-tert-butyl-2-hydroxy-1,3-benzenedicarbaldehyde with 1,2-phenylenediamine was synthesized. The molecular structure of 4 was determined by X-ray diffraction revealing a sandwich-type structure as depicted by Figure 2. Electrochemical investigations (DCV measurements) showed two one-electron reduction steps for the copper ions at E1/2 = -1.383 and -1.652 V (vs. Cp2Fe/Cp2Fe+).
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  • 264
    ISSN: 0009-2940
    Keywords: Ring enlargement reactions ; Spirocyclic cobaltaphosphazene ; Eight-membered carbon-free inorganic rings ; Tetrahedral CoE4 core (E = O, S, Se) ; Phosphazenoid skeleton ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemistry of Polyfunctional Molecules, 112.  -  Ring Enlargement Reactions of a Spirocyclic Cobaltaphosphazene with Oxygen, Sulfur, and SeleniumHerrn Prof. Dr. Ekkehard Lindner zum 60. Geburtstag gewidmet.The spirocyclic cobaltaphosphazene 1 which contains cobaltconnected three-, five-, and six-membered rings undergoes ring enlargement reactions by treatment with O2, S8, and Se8. The resulting paramagnetic spirocyclic cobalta-phosphazenoids 2a-c (E = O, S, Se) consist of eight-membered chelate rings connected at the spiro-cobalt(II) centre forming a tetrahedral CoE4 core. The compounds 2a-c have been characterized by X-ray analyses, 1H, 13C(1H), 31P(1H) NMR, IR, Raman, UV/Vis/NIR, EI/FD mass spectroscopy, and magnetic measurements.
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  • 265
    ISSN: 0009-2940
    Keywords: Selenadiphosphiranes ; Selenatriphosphetanes ; Molecular dynamics ; Phosphacycles ; Selenium compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pentamethylcyclopentadienyl-Substituted Selenadiphosphirane and Selenatriphosphetane: Synthesis, Structure, Dynamic, and Some ReactionsHerrn Prof. R. Schmutzler zum 60. Geburtstag gewidmet.1,2,3-Tris(pentamethylcyclopentadienyl)cyclotriphosphane (1) reacts with selenium to form the insertion product 2,3,4-tris(pentamethylcyclopentadienyl)selenatriphosphetane (2), which is trapped as the selenium-coordinated pentacarbonylchromium complex 4. Compound 4 is the first isolated selenatriphosphetane complex. Reaction of 2 with selenium yields 2,3-bis(pentamethylcyclopentadienyl)selenadiphosphirane (3). 3 replaces thf of Cr(CO)5thf to give the chromium complex 5. The reaction of 3 with K[Fe(CO)2Cp*] leads to the substitution product 6 and the bicyclic phosphane 7. The X-ray structures of 3 and 4 are presented. The dynamic behavior of 3-6 is discussed.
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  • 266
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1031-1035 
    ISSN: 0009-2940
    Keywords: Lithium-(fluorosilyl)phosphanides ; Phosphanides, lithium-(fluorosilyl)(phosphanyl)- ; Silylidenephosphanes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Evidence for a Structure-Reactivity Relationship of Crowded Substituted Lithium (Fluorosilyl)phosphanidesThe molecular structures and the reactivity of the new solvated lithium (fluorosilyl)phosphanides 1a, 2a, and 2b has been investigated. The unusual solid state structures of 1a and 2b are established by X-ray crystallography. Whereas the lithium centre in 1a is bound to phosphorus and solvated by three molecules of THF, the electronical saturation of the lithium centre in 2b is achieved by a Li—P bond, tridentate chelatization (fluorine, phosphorus, nitrogen), and the additional coordination of one molecule of THF. The trigonal-planar geometry at phosphorus in 1a is unprecedented for derivatives of this type and reflects the steric demand around the phosphorus and the possibility of πp/σ*sic hyperconjugation. The Si—P bond lengths [P—SiC(Phenyl) 2.186(2) and P—SiF 2.164(2) Å] are significantly shorter than in related pyramidally configurated derivatives (1b, c: P—SiC 2.21, P—SiF 2.18 Å). Both phosphorus atoms in 2b are pyramidally coordinated, but the intramolecular chelate coordination of the lithium centre causes much smaller bonding angles at the Si—P phosphorus atom [sum of bonding angles 238.4(2) (PSi), 312.5(1)° (PN)]. 1a as well as 2a, b show quite different reactivity as compared to 1b-d due to their unusual structures. Heating of solutions of 1a and 2a, b in toluene or hexane does not give the expected stable silylidenephosphanes (Si=P) by elimination of LiF. Instead, rearrangement reactions of the Si=P intermediates 6, 8 lead to the new heterocycles 5, 9. A single-crystal X-ray diffraction analysis of 5 has been performed. The Si2P2 cyclobutane ring is planar, and the NMe2 groups at the ring silicon atoms are cis-orientated.  -  Interestingly, 2b eliminates LiNiPr2 at 20°C in a kinetically controlled process to form the tetraphosphacyclobutane 7 as the major product. Presumably, the diphosphene 8 is an intermediate in this reaction.
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  • 267
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1037-1039 
    ISSN: 0009-2940
    Keywords: Borolanes ; Boroles, 2,5-dihydro ; 3,7-Diborabicyclo[3.3.0]oct-1(5)-enes ; 2,5-Diborapentalenes, 1,2,3,4,5,6-hexahydro- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 3,4-Dimethyleneborolanes and 3,7-Diborabicyclo[3.3.0]oct-1(5)-enesThe tetramethyleneethane derivative K2[C2(CH2)4] which is readily prepared from 2,3-dimethylbutadiene by metallation with the Lochmann-Schlosser base reacts with BC12(NR2) (R=Me, Et, iPr) to give the highly reactive, liquid 1-(dialkylamino)-3,4-dimethyleneborolanes (3). These dienes react with activated magnesium to give soluble magnesium adducts 5 which upon treatment with BC12(NR2) (R = Me, iPr) yield crystalline 3,7-bis(dialkylamino)-3,7-diborabicyclo-[3.3.0]oct-1(5)-enes (4). The crystal structure of the dimethyl-amino compound 4a was determined by X-Ray-diffraction. The molecule of 4a shows crystallographic C2h symmetry with an almost perfectly planar skeleton.
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  • 268
    ISSN: 0009-2940
    Keywords: Osmium(II) complexes ; Alkyl(carbonyl)hydrido complexes ; Allylhydrido complexes ; Fragmentation, metal-initiated ; C—H Activation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Studies on C—H Activation, X.  -  Synthesis of Alkyl(carbonyl)hydrido- and Allylhydridoosmium Complexes by Metal-initiated Fragmentation of Primary Alcohols and OlefinsHerrn Professor Dr. E. Lindner zum 60. Geburtstag gewidmet.The reaction of [(Mes)OsCl2]n (1) with RCH2OH/NaOH in the presence of propene leads to complete fragmentation of the primary alcohol and formation of the alkyl(carbonyl)hydrido complexes [(Mes)OsH(R)(CO)] (2-7). The corresponding chloro derivatives [(Mes)OsC1(R)(CO)] (8-13) are obtained either by H/C1 exchange from 2-7 and CC14 or on treatment of [(Mes)OsR2(CO)] (16-21) with HC1 at -78°C. The carbonylosmium(II) compound [(Mes)Os(CO)C12] (15) reacts with iC4H9MgI to give a mixture of [(Mes)Os(iC4H9)2(CO)] (21), [(Mes)OsI(iC4H9)(CO)] (22), and [(Mes)Os(CO)I2] (23), whereas the reaction of 15 with C6H11CH2MgBr yields [(Mes)Os(CH2C6H11)2(CO)] (24), the olefin complex [(Mes)Os(CH2=C6H10)(CO)] (25), and [(Mes)OsH(Br)(CO)] (26). The alkylhydridoosmium(II) compound [(Mes)OsH(CH2C6H11)(CO)] (28) is obtained from the chloro derivative 27 and Mg/Hg/C2H5OH. Treatment of 1 with iC3H7OH/NaOH and propene or isobutene affords the η3-allylhydrido complexes [(Mes)OsH(η3-2-RC3H4)] (31, 32) in about 85% yield, while the reaction of 1 with iC3H7OH/NaOH and tert-butylethene gives [(Mes)Os(CH2=CHtC4H9)2] (35). The X-ray structural analysis of [(Mes)OsH(η3-2-CH3C3H4)] (34), which like the corresponding η3-allylchloro compound 33 is formed from the η3-allylhydrido complex 31 or 32 and CC14, reveals a half sandwich-type structure with an exo arrangement of the methallyl ligand.
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  • 269
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1003-1013 
    ISSN: 0009-2940
    Keywords: Metallocene complexes, bent ; Titanium complexes ; Vinylidene complexes ; Transition metal complexes ; Heterodinuclear complexes ; Carbene complexes ; Early-Late heterodinuclear complexes ; Metallacycles ; Oxatitanacyclobutane complexes ; Oxatitanacyclopentene complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclic Isomeric Four- and Five-Membered Heterodinculear Carbene Complexes  -  Formed from a Titanocene Vinylidene Fragment and Metal CarbonylsThe four-membered heterodimetallic carbene complexes Cp*2 16 [LnM: Cr(CO)5 (a), Mo(CO)5 (b), W(CO)5 (c), CpRe(CO)2 (f), Mn2(CO)9(g), Re2(CO)9 (h), Fe(CO)4 (i), Rh(acac)(CO) (i)] are easily prepared by trapping the vinylidenetitanocene [Cp*2Ti=C=CH2] fragment 6 with the corresponding metal carbonyls. The vinylidenetitanocene 6 is generated in a favourable manner from Cp*2Ti(CH3)CH=CH2 (13) or Cp * (Fv)TiCH = CH2 (14) [Fv: C5(CH3)4CH2] by a 1,3-H shift (α elimination) at room temperature. The formation of 16 is characterized by a preferred suprafacial [2 + 2] cycloaddition. Starting from Cp*2 (5) or 14 and transition metal carbonyls unexpected isomeric five-membered titanacycles Cp*2 8 [MLn = a-c, MnCp(CO)2 (d), MnCp′(CO)2 (e), f-i] are obtained at higher temperatures (70-100°C). These oxatitanacyclopentenes 8 are formed also upon heating via the kinetic product 16 with high yield, as a result of a 1,2-hydrogen shift, proved for c, g, h. From the spectroscopic data an η1-vinylcarbene structure is deduced, exhibiting a cis- (16) or trans-configurated (8) LnM=C—C=C sequence. An X-ray structure analysis shows the importance of the acyl resonance form in 8a, typically observed for such heterodimetallic carbene complexes. The reversible liberation of the metal carbonyl is a remarkable property of complexes 16 in solution, whereas the thermodynamic product 8 shows the typical properties of Fischer carbene complexes.
    Additional Material: 1 Ill.
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  • 270
    ISSN: 0009-2940
    Keywords: λ3-Phosphaalkyne, 2-amino- ; PE Spectroscopy ; Calculations, ab initio ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactive E=C(p-p)π-Systems, XXXVIII.  -  Molecular and Electronic Structure of 2-(Diisopropylamino)-1λ3-phosphaethyne iPr2NC≡PThe molecular structure of 2-(diisopropylamino)-1λ3-phosphaethyne iPr2NC≡P (3) has been investigated by X-ray diffraction using a single crystal grown from the melt at -50.2°C. Bond distances and angles indicative for the electronic structure are: P°C 155.2(2), N—C(sp) 131.2(3) pm, P—C—N 179.2(2)°; with a sum of angles 359-8° the nitrogen atom has a trigonal-planar coordination. The reported geometrical parameters of 3 have been reproduced by ab initio calculations (3-21G and DZP basis), showing that the lengthening of the P°C and the shortening of the C—N bond can be rationalized by the interaction of the π system of the triple bond with the 2p orbital at N. The He(I) photoelectron spectrum of 3 confirms the strong interaction.
    Additional Material: 4 Ill.
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  • 271
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    Keywords: 1,2-Benzodiborete, 1,2-dihydro- ; Dibenzo[c,g][1,2,5,6]tetraborocine, 5,6,11,12-tetrakis(diisopropylamino)- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Structure of 5,6,11,12-tetrakis(diisopropylamino)-5,6,11,12-tetrahydrodibenzo[c,g][1,2,5,6]tetraborocineHerrn Prof. Dr. Gottfried Märkl zum 65. Geburtstag gewidmet.Catalytic dimerization of 1,2-bis(diisopropylamino)-1,2-dihydro-1,2-benzodiborete (1) with (phthalocyanine)palladium [Pd(pc)] leads to the eight-membered title compound 2 in 95% yield. An X-ray structure analysis of 2 exhibits a chair conformation for the central C4B4 ring (folding angle along B1B2/B1′B2′ 55.5°).
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  • 272
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1069-1073 
    ISSN: 0009-2940
    Keywords: Free-radical additions ; Alkyl radicals ; Stereoselectivity ; Hydrogen transfer ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The addition of cyclohexane to alkylmaleic anhydrides 1a-f via cyclic radicals 2a-f gave a mixture of (Z)- and (E)-2,3-dialkylsuccinic anhydrides 3a-f. The stereoselectivity of the hydrogen transfer from cyclohexane to radicals 2a-d was measured in the temperature range of 200-260°C, and the relative activation parameters of the formation of (Z)- and (E)-3 were determined. The stereoselectivity of the hydrogen transfer from cyclohexylmercuric hydride at 25°C was measured as well. The results are rationalized assuming steric interactions in the transition state of H donor and β substituent and of α and β substituent, respectively. An X-ray structure analysis of the highly strained addition product (Z)-3d was performed.
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  • 273
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    Keywords: Cyclopropyl building blocks ; Strained compounds ; [4 + 2] Cycloaddition ; Regioselectivity ; Epoxides, regioselective cleavage of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1-Ethoxy- (8a) and 1-(trimethylsilyloxy)-1,3-pentadiene (8b) cycloadded to 2-chloro-2-cyclopropylideneacetate 6 to give low yields of endo/exo-9a and -9b, respectively. On the other hand, furans 5a-d added 6 (5b and 5d reacted regioselectively) to afford mixtures of the corresponding [4 + 2] cycloadducts endo-11a-d and exo-11a-d in good to high yields. 2-Methyl-5-(trimethylsilyloxy)furan (5e) yielded a mixture of the four cycloadducts endo/exo-11e and endo/exo-12e, which upon attempted purification on silica gel underwent facile hydrolysis to give bicyclic hemiacetals endo/exo-13 and 4-hydroxycyclo-2-hexen-1-ones endo/exo-14, respectively. Similarly endo/exo-11f, and endo/exo-12f, obtained from 2-methoxy-5-methylfuran (5f) and 6, upon hydrolysis in the presence of silica gel gave endo/exo-13 and endo/exo-14 respectively. The structures of endo-14 and exo-12f were established by X-ray crystallography. In the presence of florisil, the epoxides endo-and exo-16 were formed from trimethylsilyloxy-substituted cycloadducts endo/exo-11e. Selective reduction of the α-chlorocarboxylate functionality in the cycloadducts endo-11a-d,f with LiBH4, followed by base-catalyzed cyclization of the resulting chlorohydrins endo-21a-d, f yielded the corresponding epoxides endo-22a-d,f in 22-73% overall yield. Under identical conditions, the cycloadducts exo-11a-f could not be reduced to the corresponding chlorohydrins exo-21a-f. Regioselective reduction of the acetal epoxide endo-22f to the tertiary alcohol endo-23f was achieved with sodium dihydrobis(2-methoxyethoxy)aluminate (Red-Al®). On stirring with moist silica gel, the bicyclic acetals endo-22d,f and endo-23f cleanly hydrolysed to the highly substituted spiro[2.5]oct-6-en-5-ones endo-24d,f (26 and 24% overall yields, respectively, in four steps from 5d,f and 6) and endo-25f, respectively (23% overall yield in five steps from 5f and 6).
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1065-1068 
    ISSN: 0009-2940
    Keywords: Acetals ; Amphiphiles ; Carbohydrates ; Glucosides ; Liquid crystals ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two new systems of liquid crystalline glucose derivatives 5a-d, 6a, b are prepared, studied and compared with reference compounds. The α- and β-D-dodecyl glucofuranosides 6a, b show smectic A phases. The clearing points of the furanosides are of the same magnitude as those of the pyranosides. The alkyl glucose acetals 5a-d show columnar discotic phases. The clearing points are about 30°C lower than those of the corresponding thioacetals.
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  • 275
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1091-1093 
    ISSN: 0009-2940
    Keywords: anti-Bredt Olefins ; Bicyclo[8.2.2]tetradeca-1(13),11-diene ; Photocyclization ; Tricyclo[8.2.2.012,13]tetradec-10-ene ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and photochemical generation of the octamethylene-bridged 1,3-cyclohexadiene and bicyclo[3.1.0]hexene derivatives 1 and 2, which are to be classified as anti-Bredt olefins, are reported. out Orientation of the octamethylene bridge at the sp3-hybridized bridgehead atom of 1 generates strain effects while in orientation of the bridge in 2 does not give rise to deformations of the bicyclo[3.1.0]hex-2-ene subunit. X-ray analyses indicate a twisted double bond (12.2 and 15.0°) at the bridgehead atom of 1 and a deformation of the six-membered ring from an ideal boat conformation. In contrast, the five-membered ring of compound 2 is planar. The folding angle between the five- and the three-membered ring is 111.8(2)°. The olefinic carbon atoms of 1 are slightly pyramidalized.
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  • 276
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    Keywords: Cross coupling ; iron-catalyzed ; Propargylbicyclo[1.1.0]butanes ; Allenylbicyclo[1.1.0]butanes ; Allylbicyclo[1.1.0]butanes ; [4.1.1]Propella-2,4-diene ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several uncatalyzed and transition metal-catalyzed cross coupling reactions of the Grignard compounds 1c or 2c with propargylic or allylic halides were investigated. Fe(acac)3 was the most effective catalyst for the preparation of allyl-and propargylbicyclo[1.1.0]butanes 7 and 5. In the latter case, the formation of the isomeric allenylbicyclo[1.1.0]butanes 6 was also observed. Stereoelectronic factors of substituents like a trimethylsilyl group as a directing group could be utilized for the formation of either 5 or 6. A number of bicyclo[1.0.0]butanes 15-21 with two substituents in the bridgehead positions were accessible by that route as well. In the case of the bis-allenyl compound 24c, an ene-type reaction leading to the first known derivative of a [4.1.1]propella-2,4-diene 25 was observed. Base-catalyzed isomerizations of the propargylbicyclo[1.1.0]butanes 5 opened a new route to alkynylbicyclo[1.1.0]butanes 30-32.
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  • 277
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1111-1113 
    ISSN: 0009-2940
    Keywords: Thianthrene 5-oxide ; Dioxiranes ; Hydrogen peroxide ; Oxidation ; Oxygen transfer ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thianthrene 5-oxide (SSO) is established as a useful and convenient chemical probe to assess the electronic character (Xso) of oxygen transfer agents. Thus, H2O2 under basic conditions (HOOH/nBu4NOH) gives an Xso value of 1.00, while H2O2 under acidic conditions (HOOH/HClO4) affords an Xso value near zero. On this Xso scale, dimethyldioxirane (Xso = 0.13 at 0°C) and methyl(trifluoromethyl)dioxirane (Xso = 0.10 at 0°C) are, as expected, definitely strong electrophilic oxidants.
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  • 278
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    Keywords: Heats of formation ; Bond cleavage ; C—C ; kinetics of ; Radicals ; stability of ; Correlation between heats of vaporization and solvent-accessible surfaces ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From thermochemical measurements the heats of formation ΔH0f(g) forfluorene (1), 9-methylfluorene (2), 9,9′-bifluorenyl (5), and 9,9′-dimethyl-9,9′-bifluorenyl (6) were determined. The homolytic cleavage of the dimers 5 and 6 to 9-fluorenyl (3) and 9-methyl-9-fluorenyl radicals (4), respectively, was studied in mesitylene with thiophenol as trapping agent and found to follow first-order kinetics. The activation parameters ΔH≠(5) = 212.6 (±2.1) kJ mol-1, ΔS≠(5) = 70.3 (±4.2) J mol-1 K-1 ΔH≠(6) = 164.9 (±0.7) kJ mol-1, and ΔS≠(6) = 88.2 (±1.9) J mol-1 K-1 were obtained. For 3 and 4 the radical stabilization energies RSE(3) = 67 (±7) kJ mol-1 (relative to isopropyl) and RSE(4) = 64 (±8) kJ mol-1 (relative to tert-butyl) were determined by a comparison with the activation parameters of the thermolysis of alkanes possessing the same strain enthalpy. The heats of formation for 3 and 4 and the C-H bond dissociation energies for the C-H bond in the 9-position of 1 and 2 were determined to be ΔH0f(g,3) = 300 kJ mol-1, Δ0f(g,4) = 268 kJ mol-1, BDEC—H(1) = 343 and BDEC—H(2) = 338 kJ mol-1 (estimated errors correspond to those of the RSE values). A good correlation between the heats of vaporization of 37 aromatic hydrocarbons and their calculated solvent-accessible surfaces was demonstrated. Hence, a new method to estimate heats of vaporization was established.
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1105-1110 
    ISSN: 0009-2940
    Keywords: 3-Borabicyclo[3.3.1]nonanes ; 7-[(dialkylamino)methyl]- ; 2-Azonia-1-boratatricyclo[4.3.1.14,8]undecanes ; Borane-amine complex formation ; Photoelectron spectra ; Conformational analysis ; Transanular interaction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The endo-7-[(dialkylamino)methyl]-3-borabicyclo[3.3.1]nonanes 1 and 2 have been synthesized and their intramolecular complex formation of the corresponding 2-azonia-1-boratatricyclo[4.3.1.14,8]undecanes 3 and 4 has been studied in the gas phase by UV photoelectron spectroscopy and in solution by 11-NMR spectroscopy. Deviations of the characteristic spectral features from those of the monofunctional bicyclic boranes 5 and amines 6 and 7 indicate that in the gas phase the (dimethylamino)boranes with a B-alkyl substituent adopt the tricyclic form 3a-c whereas the diethylamino and the B-methoxy derivatives 1e and 2 prefer the bicyclic structure. In solution some deviations from this behavior are observed.
    Additional Material: 3 Ill.
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  • 280
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1125-1130 
    ISSN: 0009-2940
    Keywords: Indoles, 2-aryl- ; Titanium graphite ; Zindoxifene ; Tumor-growth inhibitors ; Alkylidenation, intramolecular ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Highly reactive titanium on graphite is used to reductively cyclize electron-rich acylamino carbonyl compounds 7, 8, 12, 14, and 16 to the corresponding indole derivatives 9, 10, 13, 15, and 17. Compound 9b is a known precursor of the mammary tumor-inhibiting compound zindoxifene (2). The other products are new analogues of this anticancer drug, exhibiting the substitution pattern previously recognized to be essential for high pharmacological activity.
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  • 281
    ISSN: 0009-2940
    Keywords: Difluorometacyclophanes ; syn-Metacyclophanes ; Through-space F,F spin coupling ; X-ray structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The close approach of the fluorine nuclei in the difluorinated syn-[3.3]metacyclophanes 1, 2 and their [2.2] analogues 3, 4 leads to strong 19F,19F spin-spin interactions which obey a through-space mechanism. The geometries of 1-4 were estimated by MM2 molecular mechanics computations, those of 1 and 3 were also determined by X-ray structural analyses. The decrease of the F,F internuclear distance in the series 1, 2, 3, 4 (2.78-2.48 Å) correlates with an increase of J(FF) from +42.1 to +99.2 Hz. It follows that, for a given distance d(FF), J(FF) is up to twice as large as a previous empirical correlation has assumed and even larger with respect to earlier theoretical calculations. Only weak F,F spin interaction occurs in 8, the anti isomer of 4.
    Additional Material: 5 Ill.
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  • 282
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1115-1118 
    ISSN: 0009-2940
    Keywords: Epoxidation ; Dioxirane, dimethyl- ; Benzofurans, 2,3-dimethyl- ; Benzofuran epoxides ; Quinone methides ; [2 + 2] Photocycloaddition ; Benzoxetes ; Hetero-Diels-Alder reaction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Irradiation (λ 〉 366 nm) of the quinone methides 3, which were formed by valence isomerization of the methyl-, chloro-, and tert-butyl-substituted 2,3-dimethylbenzofuran epoxides 2, afforded the novel 2H-benzoxetes 4 by photochemical [2 + 2] cycloaddition. These strained and highly labile benzoxetes 4 were spectrally (1H and 13C NMR) characterized at subambient temperatures. On prolonged storage (2-3 d) at -20 to -10°C, the benzoxetes 4 reverted to the quinone methides 3 and/or benzofuran epoxides 2.
    Additional Material: 1 Tab.
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  • 283
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1143-1145 
    ISSN: 0009-2940
    Keywords: Fulvenes ; Norbornadienes ; Cycloadditions ; Diels-Alder reactions ; Pyrolysis, flash vacuum ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of Methyl 6,6-Dimethylfulvene-2-carboxylate and Dimethyl 6,6-Dimethylfulvene-2,3-dicarboxylate as well as their Reaction to 2,3,5,6-Substituted NorbornadienesFulvenes 5 and 6 were synthesized by Diels-Alder reaction of 6,6-dimethylfulvene with methyl prop-2-ynoate and dimethyl but-2-ynedioate, catalytic reduction of the unsubstituted norbornadiene double bond, and a subsequent retro Diels-Alder reaction under flash vacuum pyrolysis conditions, 5 and 6 are used as the diene component in synthesizing 2,5-, 2,3,5-, and 2,3,5,6-substituted norbornadienes 7-9 by Diels-Alder reaction with electron-deficient alkynes.
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  • 284
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1137-1142 
    ISSN: 0009-2940
    Keywords: Isoquinolines, hexahydro- ; Cyclobuta[c]pyridines, hexahydro- ; Cycloadditions, [2 + 2]- and [4 + 2]- ; 3-Azabicyclo[3.1.0]hexane, 6,6-dibromo-3-phenyl- ; 2,4-Pentadienylamine, 3-n-butyl-N-phenyl- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cycloallenes, 9.  -  1-Phenyl-1-aza-3,4-cyclohexadiene, the First Isodihydropyridine: Generation and InterceptionThe generation of the title cycloallene 4 from 6,6-dibromo-3-phenyl-3-azabicyclo[3.1.0]hexane (10) with methyllithium according to the Doering-Moore-Skattebøl method is reported. In the presence of styrene, 1,3-butadiene, furan, 1,3-cyclohexadiene, and 1,3-cyclopentadiene, 4 is intercepted in [2 + 2] and [4 + 2] cycloadditions with formation of the hexahydrocyclobuta[c]pyridines 6 and 11 and the hexahydroisoquinolines 12-15, respectively. The starting compound 10 is prepared via the cis-disubstituted 1,1-dibromocyclopropanes 8 and 9 from the known dioxepine derivative 7, the synthesis of which has been considerably improved. On treatment with n-butyllithium, the dichlorophenylazabicyclohexane 3 is converted into 4 as well. However, in the competition for 4, styrene is not successful against n-butyllithium, which transforms 4 into the pentadienylamine 5.
    Additional Material: 2 Tab.
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  • 285
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1147-1156 
    ISSN: 0009-2940
    Keywords: Adamantanes ; Adamantanophanes ; Cyclophanes ; Ring strain ; Sulfone pyrolysis ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Preparation, Structure, and Conformational Behaviour of Strained AdamantanophanesExchange of aromatic units (e.g. benzene) for aliphatic/alicyclic building blocks (e.g. adamantane) in cyclophanes leads to new molecules of the “araliphane” type. In the framework of this concept the araliphanes 3(a), 5-7a, 10(a), and 11 are synthesized. Their stereochemical behaviour differs significantly from that of their aromatic counterparts as shown by NMR studies and X-ray crystallographic analyses. Extremely upfield-shifted signals of the intraanular adamantane hydrogen atoms are found as well as a planar chiral adamantanophane. A Diels-Alder addition of 8 to the benzene ring of 6 yields 9. Complete replacement of benzene units by adamantane leads to the fully aliphatic/alicyclic “aliphanes”. The crystal structure of 15 is described.
    Additional Material: 6 Ill.
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  • 286
    ISSN: 0009-2940
    Keywords: Electrophilic vinylic substitution ; Isocyanates ; α,β-Unsaturated amides, synthesis of ; Carbodestannylation ; Alkenylstannanes, applications of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new and effective method for the preparation of a variety of olefinic carboxamides 6a-k and N-(4-methylphenyl-sulfonyl) carboxamides 7a-d is described. The reaction of aryl and alkyl isocyanates 4a-c or 4-methylphenylsulfonyl isocyanate 5 with 1-alkenyltrialkylstannanes 1a-e and di-1-alkenyldibutylstannanes 2a-c in the presence of aluminium trichloride provides the corresponding N-aryl-substituted olefinic carboxamides 6a-k or the N-(4-methylphenyl-sulfonyl)-substituted olefinic carboxamides 7a-d in good yields. The stannyl moiety is superior to hydrogen as a leaving group and enables electrophilic ipso substitution at the vinylic system. In the case of di-1-alkenyldibutylstannanes the substitutions are also stereospecific, whereas the reactions of 1-alkenyltrialkylstannanes with isocyanates proceed with partial isomerisation.
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  • 287
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1157-1162 
    ISSN: 0009-2940
    Keywords: Cyclophanes ; Naphthalenophanes ; McMurry reaction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The (1,4)naphthalenophanes 6a, 6b, 7a, and 7b were synthesized regiospecifically in two steps from the appropriate α,β-di-1-naphthylalkanes by a Friedel-Crafts acetylation of the two naphthalene groups followed by cyclization/dimerization of the resulting diketones by a McMurray reaction. The macrocyclic naphthalenophanes 6a and 6b exist in solution as a mixture of conformers while 7a and 7b were identified as the anti isomers.
    Additional Material: 2 Ill.
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  • 288
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1167-1170 
    ISSN: 0009-2940
    Keywords: Annulenes ; Chromophores ; Hexatrienes ; Hydrocarbons ; Macrocyclic compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The [6.6]cyclophanehexaene hydrocarbon 6a and the dimethoxy[6.6]cyclophanehexaene 6b are prepared starting with the unsaturated diacid 1. An X-ray analysis of 6a exhibits a planar molecular skeleton. NMR and optical data prove a not fully conjugated macrocyclic π system and its division into two largely separate chromophores.
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  • 289
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1163-1166 
    ISSN: 0009-2940
    Keywords: Cyclophanes ; Coupling reaction ; McMurry reaction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The [2.1.2.1]paracyclophanedienes 9-11 were prepared in good yields by a McMurry cyclization of the bis(4-acylphenyl)methanes 5 and 6 and of bis(4-acetylphenyl) ether (7), respectively.
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  • 290
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1171-1173 
    ISSN: 0009-2940
    Keywords: Tandem mass spectrometry ; Collision experiments ; Sulfur-nitrogen clusters ; Electron transfer ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Collision experiments on NS-x (x = 2, 3) clusters are reported. Evidence is presented for the gas-phase existence of the corresponding NS.x and NS+x species. For x = 3, the mass spectra are very much in keeping with a connectivity SS-NS (5) for all three charge states. For x = 2, the experimental data favor the presence of NSS (2); however, the cyclic C2v-symmetric form 3 cannot be ruled out.
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  • 291
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    Berichte der deutschen chemischen Gesellschaft 127 (1994) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 292
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. A65 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 293
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1177-1183 
    ISSN: 0009-2940
    Keywords: Phosphorus ylides ; Olefination reactions ; Mercury compounds ; Vinyl compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of novel α-mercurio-substituted phosphorus ylides, Ph3P=CR[HgN(SiMe3)2] 3a-d (R = Me, Et, iPr, Ph) is easily accomplished by mixing equivalent amounts of a phosphorus ylide 1a-d with Hg[N(SiMe3)2]2 in an inert solvent. These organometallic compound are completely characterized including an X-ray analysis of 3a. Their reaction with benzaldehyde yields vinylmercury amides (E)/(Z)-PhHC=CR[HgN(SiMe3)2] 4a-d. In reactions involving 3a-c the stereochemistry [favored formation of (E)-4a (≍;72 - 83%) and (Z)-4b, c (≍60 - 73%)] in the absence of a lithium salt is contrary to the stereochemistry of the established Wittig olefination reaction with non-stabilized phosphorus ylides like 1a-d. From the reported results, the preliminary conclusion is drawn that the stereochemistry is mainly controlled by steric interactions. Only in one case a remarkable salt effect is observed. When 3c reacts with benzaldehyde in the presence of LiBr and THF as solvent up to 95% of (E)-4c is formed. The semistabilized ylide 3d gives under all conditions studied a 50:50 mixture of (E)/(Z)-4d. The vinylmercury amides 4a, c are cleaved by hydrous NaOH to yield divinyl-mercury compounds (E,E)-(PhHC=CR)2Hg and (Z,Z)-(PhHC=CR)2Hg (R = Me: 7a; R = iPr: 7c). The compound 4d is cleanly cleaved by NaBH4 in hydrous 3 M NaOH to yield a 50:50 mixture of cis- and trans-stilbene (8).
    Additional Material: 1 Ill.
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  • 294
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1185-1190 
    ISSN: 0009-2940
    Keywords: Dyes ; Colour and constitution ; Halochromism ; Alizarin ; Purpurin ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Constitution and Colour of Alizarin and Purpurin DyesThe colour of madder dyes used as pigment in antiquity and in the last centuries is produced mainly by metal complexes of alizarin (1) and purpurin (2). Single crystals of aluminium calcium alizarinate and purpurinate are obtained by two-phase crystallization. X-ray structure determinations show tetranuclear complex molecules with four alizarins which are different from formerly proposed structures. Solutions of 17 metal complexes of alizarin in DMF/Water exhibit UV-Vis spectra the maxima of absorption of which strongly depend on the electronegativity of the metals. A classical explanation for this is given.
    Additional Material: 6 Ill.
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  • 295
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    Keywords: Ethylboronic carboxylic acid anhydrides, comproportionation of ; Bicyclo[3.3.1]nonadienes, heteroatom-containing ; Bicyclo[3.3.3]undecadienes, heteroatom-containing ; 1,3,2-Diboroxanes ; Oxygen atom exchange ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chelate-Stabilized 1,3-Bis(acyloxy)-1,3-diethyldiboroxanes from Triethylboroxin and Carboxylic Acid AnhydridesTriethylboroxin (A) reacts with carboxylic acid anhydrides (RCO)2O [R = Me: 1a; Et: 1b; tBu: 1d; Ph: 1e] with various rates to give high yields of the 3,7-dialkyl-1,5-diethyl-4,8,9-trioxa-2,6-dioxonia-1,5-diboratabicyclo[3.3.1]nona-2,6-dienes OB(Et)OC(R)OB(Et)OC(R)O (2) [R = Me: 2a (X-ray crystal structure analysis); Et: 2b; tBu: 2d; Ph: 2e], presumably via the unstable compounds OB(Et)OB(Et)OC(R)OB(Et)OC(R)O (3a,b, d, e). Compound 1c (R = CF3) reacts with A to form a mixture of 1,3-diethyl-1,3-bis(trifluoroacetoxy)diboroxane O=C(CF3)OB(Et)OB(Et)O(CF3)C=O (2c′) and 2c (R = CF3) at room temperature. Whereas two compounds of the type 2 do not comproportionate, 1a-e spontaneously form the mixed substituted carboxylic acid anhydrides 1ab etc. on mixing at room temperature (GC, 13C NMR). - From the 17O-enriched A* and 1a-e the 17O-enriched compounds 2a*-e* with BO*B and YYBO*OCR groups are obtained. A* exchanges O atoms up to 200°C with succinic anhydride (1f) forming 1f* or with phthalic acid anhydride (1g) forming 1g* and 3g*. - The mixed carboxylic acid anhydrides 1xy are cleaved, and the mixtures of 1 are separated with A to yield the uniform 3,7-dialkyl-substituted compounds 2.
    Additional Material: 2 Ill.
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1213-1218 
    ISSN: 0009-2940
    Keywords: Silicon ; Octahedral oxygen coordination ; Phosphorus ; NMR, 1H MAS ; NMR, 29Si MAS ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A Simple Route to Silicon in Octahedral Oxygen CoordinationSyntheses and crystal structures of three new compounds Rb2SiP4O13 (1), Cs2H2Si(P2O7)2 (2), and BaH2Si(P2O7)2 (3) containing silicon in an octahedral oxygen coordination are reported. The structures have been determined by X-ray structure analyses. All three compounds are constituted of silicophosphate polyanions. The NMR chemical shifts of silicon and hydrogen are measured.
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  • 297
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    Keywords: Oxo complexes ; Imido complexes ; Borato, tris(3,5-dimethyl-1-pyrazolyl)hydrido complexes ; Vanadium complexes ; Niobium complexes ; Tantalum complexes ; Chromium complex ; Molybdenum complexes ; Tungsten complexes ; Rhenium complex ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Higher-Valent Derivatives of the d-Metal Acids, 13.  -  Homoscorpionates as Tripodal Anchoring Ligands of Chloro Functionalized Oxo and Imido Complexes of Elements of Group 5-7Hydridotris(pyrazolyl)borate complexes of elements of group 5-7 have been prepared by reaction of d0-metalloyl chlorides [M(Y)nClm]x (Y = O, NR) with KTp* (Tp* = κ3-HB(3,5-Me2pz)3). Thus [NbOCl3]x and [TaOCl3]x are converted into monomeric and well-characterized oxo complexes [Tp* Nb(O)Cl2] (1) and [Tp*Ta(O)Cl2] (2). In a similar way [Tp* Mo(O)2Cl] (3) and [Tp*W(O)2Cl] (4) have been obtained from the oxo chlorides [MoO2Cl2]x and [WO2Cl2]x, respectively. tert-Butylamine reacts with NbCl5 and TaCl5 in the presence of pyridine to give the imido pyridine complexes [Nb(NtBu)Cl3(py)2] (5) and [Ta(NtBu)Cl3(py)2] (6) in excellent yield. Imido complexes [Tp*V(NtBu)Cl2] (7), [Tp* Nb(NtBu)Cl2] (8), and [Tp*Ta(NtBu)Cl2] (9) are formed by the reaction of KTp* with the precursers [V(NtBu)Cl3]x or 5 and 6, respectively. The corresponding imido complexes of group 6, namely [Tp*Cr(NtBu)2Cl] (10), [Tp*Mo(NtBu)2Cl] (11), and [Tp*W(NR)2Cl] (R = tBu 12a, 2,4,6-Mesityl 12b, SO2Ph 12c) are obtained directly from the imidoyl chlorides or their complexes with Lewis bases. 11 and 12 are prone to protonation at the imido ligand to yield cationic amido species [Tp*M(NtBu)(NHtBu)Cl]BF4 (M = Mo 13, W 14). Finally the preparation of cationic imido rhenium complex [Tp*Re(NtBu)2Cl]PF6 (15), isoelectronic with 10-12, is described. The molecular structure of 11 has been determined by X-ray diffraction. Despite of a maximum electron count of 20 valence electrons, all three pyrazolyl groups of the tripodal ligand are facially coordinated. In a way similar to the well-known ring slippage of analogous cyclopentadienyl complexes, the weakest bound pyrazolyl ligand is asymmetrically attached to molybdenum deviating from the positions expected for local C3v symmetry.
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 2475-2482 
    ISSN: 0009-2940
    Keywords: Vinylcarbene complexes ; Chromium complexes ; Tungsten complexes ; Phosphorus ylide complexes ; Alkynylcarbene complexes ; Allene complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alkynylcarbene complexes (CO)5M≡C(OEt)-C≡C—R 1 (M = Cr, W; R = Ph, tBu, SiMe3) readily add tertiary phosphanes PPhR2′ 4 (R′ = Ph, Me) to form stable zwitterionic phosphonium allenide complexes (CO)5M--C(OEt) = C≡C(R)-P+PhR2′ 5. Complex 5a (M = Cr, R = R′ = Ph) was characterized by X-ray diffraction. The addition of secondary phosphanes PHR2 6 to 1 affords red (2-phosphanyl ethenyl)-carbene complexes (CO)5M≡C(OEt)-CH≡C(R)-PR2 (E)-8 (R = tBu, cC6H11, Ph) in 34-89% isolated yields. Dinuclear complexes (CO)5M≡C(OEt)-CH≡C(R)-P(R2)M(CO)5 (E)-9 are obtained as byproducts. Compounds (E)-8b (M = Cr, R = cC6H11) and (E)-9i (M = Cr, R = Ph) were characterized by X-ray analyses.
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  • 299
    ISSN: 0009-2940
    Keywords: Electrophilicity ; Ferrocenylmethylium ions ; Kinetics ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Second-order rate constants for the reactions of the ferrocenylmethylium ions 2a - e with silyl enol ethers, allylsilanes, allylstannanes, and hydride donors have been determined photometrically and conductometrically in dichloromethane. The ferrocenylmethylium ions 2a - d (fc-CHR+, R = H, Me, Ph, An) are slightly stronger electrophiles than the tropylium ion, and their electrophilic reactivities depend only slightly on the nature of R. The bis(ferrocenyl)methylium ion 2e is a considerably weaker electrophile, comparable to the tricarbonyl(cyclohexadienyl)iron cation.
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 2423-2429 
    ISSN: 0009-2940
    Keywords: Triazenes, aryl ; Radical cations ; Cyclic voltammetry ; ESR spectroscopy ; UV-Vis spectroelectrochemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 3,3-Dimethyl-1-(4-R-phenyl)- [R = (CH3)2N, C2H5O, CH3O, CH3; 3] and 3-Methyl-1-(4-R1-phenyl)-3-(4-R2-phenyl)triazenes [R1 = (CH3)2N, CH3O, NO2, R2 = CH3O, H, 4] are oxidized electrochemically and chemically to their one-electron oxidation products. Cyclic voltammograms of the triazenes are discussed, and ESR as well as UV/Vis spectra of the radical cations are presented. The stability of the triazene radical cations generated depends on the substituents on the aryl rings. 4-R-Benzenediazonium ions are identified as one of the decay products of the radical cations by means of cyclic voltammetry and UV/Vis spectroelectrochemistry.
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