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1.
S. Anfang J. Grebe M. Mhlen B. Neumüller N. Faza W. Massa J. Magull K. Dehnicke 《无机化学与普通化学杂志》1999,625(8):1395-1400
Synthesis and Crystal Structures of the Phosphoraneiminato Complexes [AlCl2(NPEt3)]2, [GaI2(NPEt3)]2, and [GaI2(NPPh3)]2 [AlCl2(NPEt3)]2 ( 1 ) is made according to the known method by reaction of aluminium trichloride with the silylated phosphaneimine Me3SiNPEt3 in acetonitrile; it is isolated as colourless, moisture sensitive crystals. The phosphoraneiminato complexes [GaI2(NPEt3)]2 ( 2 ) and [GaI2(NPPh3)]2 ( 3 ), on the other hand, are obtained by redox reactions as pale yellow crystals; ( 2 ) of “gallium(I) iodide” with Me3SiNPEt3 in toluene and ( 3 ) of gallium with N-iodine triphenylphosphaneimine, INPPh3, in tetrahydrofuran. 1 and 3 are characterized spectroscopically and by crystal structure determinations; 2 is characterized only crystallographically. 1 : Space group Pbca, Z = 4; lattice dimensions at –70 °C: a = 1232.6(2), b = 1341.1(2), c = 1393.4(3) pm, R1 = 0.0315. 1 forms centrosymmetric molecules in which the Al atoms are linked via Al–N bonds of the two (NPEt3–) groups; with 185.0 and 184.4 pm these bonds are of almost the same lengths. 2 : Space group Pbca, Z = 4; lattice dimensions at –80 °C: a = 1380.0(1), b = 1311.0(1), c = 1429.1(1) pm, R1 = 0.0273. 2 crystallizes isotypically with 1 . The gallium atoms of the centrosymmetric Ga2N2 four-membered ring are connected with Ga–N distances of equal length (190.9 pm). 3 · THF: Space group P212121, Z = 2; lattice dimensions at –140 °C: a = 1494.6(1), b = 1536.3(1), c = 974.6(1) pm, R1 = 0.0382. 3 forms dimeric molecules in which the gallium atoms are linked via the N atoms of the (NPPh3–) groups to form a non-planar Ga2N2 four-membered ring of C2 symmetry with Ga–N bonds of equal lengths – within standard deviations – of 194.7 pm. The phosphoraneiminato groups are arranged in a synperiplanar way. 相似文献
2.
[reaction: see text] On the basis of KIE experiments, the ring opening of cis-bicyclo[4.2.0.]oct-7-ene has been suggested as an anti-Woodward-Hoffmann reaction candidate. We hereby report the results of a high-level computational study of the alternate reaction pathways which proves that the energy profiles show a clear preference for the conrotatory (W-H allowed) ring opening followed by double-bond isomerization. Computed KIE values for the aforementioned mechanism are in good agreement with the experimental values. 相似文献
3.
Crystal Structures of the Silylated Phosphaneimines Me3SiNP(c-C6H11)3 and (Me3SiNPPh2)2CH2 The crystal structures of Me3SiNP(c-C6H11)3 ( 1 ) and (Me3SiNPPh2)2CH2 ( 2 ) are determined by X-ray diffraction at single crystals. In both compounds the PN distances correspond to double bonds, the SiN distances to single bonds. With 149.8° the SiNP bond angle in 1 is noticeably large, while it is only 138.5° in 2 , which shows C2 symmetry. 1 : Space group P21/n, Z = 4, lattice dimensions at –70 °C: a = 1143.0(1), b = 1743.0(2), c = 1152.5(1) pm, β = 90.42(1)°; R = 0.0677. 2 : Space group I41/a, Z = 8, lattice dimensions at –60 °C: a = b = 1959.7(1), c = 1695.8(1) pm, R = 0.0433. 相似文献
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5.
Faza ON López CS Alvarez R de Lera AR 《Journal of the American Chemical Society》2006,128(7):2434-2437
The mechanism of the stereospecific gold(I)-catalyzed Rautenstrauch rearrangement of (E)-1-ethynyl-2-methyl-but-2-en-yl acetate to 3,4-dimethyl-cyclopent-2-enone has been computationally addressed using DFT (B3LYP/6-31G, SDD for Au). Our results indicate that the bond formation event follows the Au(I)-induced acetyl transfer to the vicinal alkyne and that it is the helicity of the pentadienyl cation intermediate which keeps memory of the chiral information. The fidelity of the center-to-helix-to-center chirality transfer requires that the rates of helix interconversion and pivaloyl rotation are slower than the cyclization, as calculations predict. 相似文献
6.
Ferreira BS de Almeida CG Faza LP de Almeida A Diniz CG da Silva VL Grazul RM Le Hyaric M 《Molecules (Basel, Switzerland)》2011,16(7):5875-5885
Pequi (Caryocar brasiliense Camb.), baba?u (Orbignya phalerata Mart.), buriti (Mauritia flexuosa), and passion fruit (Passiflora edulis) oils were studied to determine their antibacterial, antioxidant and cytotoxic activities, as well as their total phenol and carotenoid contents. The fatty acid contents were determined by GC-MS. The three types of passion fruit oils studied were refined, cold pressed or extracted from seeds in a Soxhlet apparatus. The oils thus obtained showed differences in antioxidant activity and carotenoid content, but were similar in regard to total phenols. Buriti and pequi had the highest carotenoid contents, while refined and cold pressed passion fruit oil displayed the highest antioxidant activity. Pequi oil was the only oil to display antibacterial and cytotoxic activity. 相似文献
7.
[reaction: see text] The species presumably involved in the associative ligand substitution mechanism for the Stille cross coupling of vinyl bromide and trimethylvinyl stannane with Pd(PMe(3))(2)/PMe(3) as catalysts in DMF (as ligand and solvent) have been structurally and energetically characterized. The cyclic four-coordinate transition state for the rate-determining transmetalation step explains the retention of configuration in the Stille coupling of chiral nonracemic alkyl stannanes. 相似文献
8.
Ulrike Riese Naim Faza Werner Massa Klaus Harms Thees Breyhan Paul Knochel Jürgen Ensling Vadim Ksenofontov Philipp Gütlich Kurt Dehnicke 《无机化学与普通化学杂志》1999,625(9):1494-1499
The phosphoraneiminato complexes [MnBr(NPEt3)]4 ( 1 ) and [M4Br5{NP(NMe2)3}3] with M = Mn ( 2 ) and M = Co ( 3 ) are prepared by melting reactions from the anhydrous metal dibromides with the silylated phosphaneimines Me3SiNPR3 (R = Et, NMe2) in the presence of potassium fluoride. All complexes are characterized by crystal structure analyses. 1 forms an only slightly distorted Mn4N4 heterocubane skeleton with an approximate Td symmetry and short Mn…Mn distances of average 295.7 pm. In the structures of 2 and 3 one μ3-NPEt3 ligand of 1 is replaced by one bromine atom with μ3-function. This leads to the novel heterocubane type M4N3Br with approximate C3 symmetry. The deformation of the cubic skeleton leads to metal-metal distances of different lengths, i. e. 292.7 and 323.6 pm in 2 and 274.4 and 306.2 pm in 3 . Temperature dependent magnetic susceptibility measurements between 300 and 5 K on 1 have shown that strong antiferromagnetic coupling exists between the Mn(II) ions with S = 5/2, with a large negative Weiss constant of Θ = –694 K. 相似文献
9.
Rocío Velasco Dr. Carlos Silva López Dr. Olalla Nieto Faza Prof. Dr. Roberto Sanz 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(42):15058-15068
By carefully controlling the reaction temperature, treatment of aryl benzyl ethers with tBuLi selectively leads to α‐lithiation, generating stable organolithiums that can be directly trapped with a variety of selected electrophiles, before they can undergo the expected [1,2]‐Wittig rearrangement. This rearrangement has been deeply studied, both experimentally and computationally, with aryl α‐lithiated benzyl ethers bearing different substituents at the aryl ring. The obtained results support the competence of a concerted anionic intramolecular addition/elimination sequence and a radical dissociation/recombination sequence for explaining the tendency of migration for aryl groups. The more favored rearrangements are found for substrates with electron‐poor aryl groups that favor the anionic pathway. 相似文献
10.
Changing the dienophile moiety of an intramolecular Diels-Alder (IMDA) cycloaddition from an allyl ether to an allenyl ether can dramatically change the regioselectivity. We hereby show by density functional theory computations that such unprecedented divergence is produced by an underlying change in the mechanism of the reaction. The allyl ether yields a fused tetrahydrofuran through a classical Diels-Alder reaction, whereas the allenyl ether yields a (methylidene)tetrahydropyran through a stepwise process. The latter reaction involves an extreme asynchronism in the bond-forming events with a diradicaloid intermediate that is stabilized by conjugation and synergistic (captodative) effects. Comparison with intermolecular model D-A reactions, which are concerted processes with various degrees of asynchrony, helps explain the change in regioselectivity for the IMDA reaction of allyl systems and the shift in mechanism for the IMDA reaction of the allenyl derivatives studied. 相似文献