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1.
Reaction of the transient phosphinidene complexes R-P=W(CO)5 with N-substituted-diphenylketenimines leads unexpectedly to the novel 2-aminophosphindoles, as confirmed by an X-ray crystal structure determined for one of the derivatives. Experimental evidence for a methylene-azaphosphirane intermediate was found by using the iron-complexed phosphinidene iPr2N-P=Fe(CO)4, which affords the 2-aminophosphindole together with the novel methylene-2,3-dihydro-1H-benzo[1,3]azaphosphole. Analysis of the reaction pathways with DFT indicates that the initially formed methylene-azaphosphirane yields both phosphorus heterocycles by way of a [1,5]- or [1,3]-sigmatropic shift, respectively, followed by a H-shift. Strain underlies both rearrangements, which causes these remarkably selective conversions that can be tuned by changing the substituents.  相似文献   
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Six novel dispirophosphirane complexes have been synthesized from the reaction of bicycloalkylidenes with the electrophilic phosphinidene complex PhPW(CO)(5). They contain a central phosphirane ring, which is spirofused on one side to a cyclopropane or cyclobutane ring and on the other side with a three-, four-, five-, or six-membered ring. Their crystal structures and MP2/6-31G-computed geometries for simplified parent systems suggest that spirofusion with small rings results in a tightening of the central three-membered phosphaheterocycle, while spirofusion with larger rings results in a relaxation of the phosphirane geometry. Similar theoretical predictions are made for the corresponding annulated hydrocarbons. Strain energies for both the hydrocarbon and phosphorus series of structures have been calculated at G3(MP2). Whereas the [3]triangulane hydrocarbon and phospha[3]triangulane have a significant excess strain of 8.1 and 5.2 kcal/mol per spiroatom, respectively, the excess strain for systems spirofused with larger rings are negligible for the hydrocarbons and even negative for the phosphorus-containing species because of hyperconjugative stabilization.  相似文献   
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Multiple applications of isothioureas as fine chemicals (or their precursors) are known, but a general sustainable method for their synthesis was hitherto unavailable. We report a novel general approach towards S‐alkyl and S‐aryl isothioureas through a copper(I)‐catalyzed three‐component reaction between amines, isocyanides, and thiosulfonates. The formal synthesis of a superpotent sweetener further illustrates the applicability of our method.  相似文献   
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Summary In a preceding publication of the present author expressions were derived to describe the pulse field from a vertical electric antenna placed near the plane boundary of two semi-infinite diëlectrics. These expressions appeared to be integrals on a finite range in the complex plane and were derived for the field in both media. The analysis of the field also gave information about the time of arrival of the several pulse-fronts.In the present paper the field is studied in more detail, and with the aid of suitable approximations more specific results are obtained, such as logarithmic field singularities.Also a discussion of the pulse analogon to the Zenneck wave in the time harmonic case has been included.  相似文献   
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Summary In a foregoing paper the present author developed methods for studying the transient field from a vertical electric antenna placed in the vicinity of the plane boundary of two semi-infinite dielectric media.As the theory involved is applicable to the comparable elastodynamic pulse problem the present paper deals with the field from a buried transient longitudinal source in an elastic half space.The method appears to be relatively simple and is also applicable to the more general problem in which two elastic semi-infinite solids are separated by a plane boundary.  相似文献   
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