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The Lewis acid-mediated reaction of alkene nucleophiles with peroxyacetals provides an effective route for the synthesis of homologated peroxides and hydroperoxides. In the presence of Lewis acids such as TiCl(4), SnCl(4), and trimethylsilyl triflate, peroxyacetals and peroxyketals undergo reaction with allyltrimethylsilane, silyl enol ethers, and silyl ketene acetals to afford homoallyl peroxides, 3-peroxyketones, and 3-peroxyalkanoates, respectively. Reactions of peroxyacetals are Lewis acid dependent; TiCl(4) promotes formation of ethers while SnCl(4) and trimethylsilyl triflate promote formation of peroxides. Lewis acid-promoted reactions of silylated hydroperoxyacetals furnish silylated hydroperoxides, which can be deprotected to homologated hydroperoxides. Hydroperoxyketals undergo Lewis acid-mediated allylation to furnish 1,2-dioxolanes via attack of hydroperoxide on the intermediate carbocation. Lewis acid-mediated cyclization of unsaturated peroxyacetals furnishes 1,2-dioxanes, 1,2-dioxepanes, and 1,2-dioxacanes through 6-endo/exo, 7-endo/endo, and 8-endo/endo pathways. The corresponding reactions involving 6-endo/endo and 5-endo/exo pathways were unsuccessful.  相似文献   
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Summary Crystal structures have been determined for two nickel complexes of the monodentate S-donating ligand 1-methyl imidazoline-2(3H)-thione (mimtH). The parainagnetic trans-octahedral complex, [Ni(mimtH)4Cl2], crystallises in an orthorhombic unit cell (a=12.459(1),b=13.078(1),c=15.406(1)Å, V=2510.24Å3,Z=4, space group Pbca). Final conventional R from 1848 observed data [F>4(F)] is 0.0273. The Ni–Cl distance is. 2.537(1) Å and the mean Ni–S distance is 2.479 Å.The diamagnetic complex, [Ni(mimtH)4](BF4)2, contains a distorted square-planar cation which is H-bonded. to [BF4] anions. The complex crystallises in an orthorhombic unit cell [a=9.810(1),b=14.585(1),c=20.120(2)Å, V=2878.8Å3,Z=4, space group Pbcn]. Final conventional R from 1756 observed data [F>4(F)] is 0.0629. The average Ni–S distance is 2.216Å.  相似文献   
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Summary Imidazoline-2-thione (imtH 2) and 1-methylimidazoline-2-thione (mimtH) react with FeCl2·4H2O in rigorously anhydrous media producing complexes of general formula Fe(LH)2Cl2.Infrared and electronic spectra as well as room temperature magnetic moments are consistent with mononuelear, pseudotetrahedral species. The crystal structure of [Fe(mimHH)2Cl2] confirms this arrangement. The complex crystallises in a triclinic unit cell (a=7.376(2),b=7.595(2),c=15.043(4) Å. =76.80(1)°, =79.60(1)°, =61.90(1)°; V=721.13 Å3; space group=P1, Z=2). Final conventional R from 2267 observed data (F >4(F)) is 0.0271. Average bond lengths are 2.353 Å (Fe–S) and 2.265 Å (Fe–Cl). Angles at the metal range from 91.5(1)° to 114.5(1)°.Thermal degradation of the complexes in flowing air involves sequential loss of halogen and ligand with -Fe2O3 as the final product. The decomposition is exothermic in flowing dinitrogen.  相似文献   
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Background  

It is well known that both semantic and syntactic information play a role in pronoun resolution in sentences. However, it is unclear what the relative contribution of these sources of information is for the establishment of a coreferential relationship between the pronoun and the antecedent in combination with a local structural case constraint on the pronoun (i.e. case assignment of a pronoun under preposition governing). In a prepositional phrase in German and Dutch, it is the preposition that assigns case to the pronoun. Furthermore, in these languages different overtly case-marked pronouns are used to refer to male and female persons. Thus, one can manipulate biological/syntactic gender features separately from case marking features.  相似文献   
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