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131.
Cycloaddition of diazoalkanes to diazabicyclo[2.2.0]hexenes and subsequent extrusion of nitrogen afford diazatricyclo[3.2.0.02,4]heptanes that are easily valence isomerized to novel dihydrodiazepines. 相似文献
132.
Wirnsberger G Pillep BM Popitsch A Knoll P Behrens P 《Chemistry (Weinheim an der Bergstrasse, Germany)》2002,8(17):3927-3937
Mercury(II) halides HgX(2) (X=Cl, Br, I) were inserted into the voids of the crystalline microporous SiO(2) modifications deca-dodecasil 3R (short term: DDR), silica-theta-1 (TON), silica-ferrierite (FER) and silicalite-1 (MFI) by vapour phase loading. The properties of the occluded guest species were studied by X-ray absorption spectroscopy (X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) analysis), UV/Vis spectroscopy, and IR and Raman spectroscopy. The methods reveal the presence of HgX(2) molecules in the insertion compounds. The interactions between these electroneutral guest molecules and the electroneutral surrounding SiO(2) framework are weak. In addition, no indication of any significant guest-guest interaction between the embedded molecules was found, in contrast to the analogous iodine insertion compounds, where these become more important with increasing pore dimensionality (G. Wirnsberger et al., Angew. Chem. 1996, 108, 2951-2953; Angew. Chem. Int. Ed. Engl. 1996, 35, 2777). Analysis of the HgL(3) EXAFS confirms a coordination number of two for Hg and gives HgX bond lengths of 2.26 +/- 0.02, 2.38 +/- 0.02 and 2.57 +/- 0.02 A for the trapped HgCl(2), HgBr(2) and HgI(2) molecules, respectively. These values are very close to those of the corresponding molecules in the vapour phase and are the shortest determined for HgX(2) molecules in solid-state compounds to date (a comparably short distance only appears in the recently reported [Cu(2-pyrazinecarboxylato)(2)HgI(2)] x HgI(2) with d(Hg[bond]I)=2.577(2) A; Dong et al., Angew. Chem. 2000, 112, 4441-4443; Angew. Chem. Int. Ed. 2000, 39, 4271). Thus, there emerges a picture of almost unperturbed HgX(2) molecules, similar to those in the vapour phase or in non-coordinating solvents, in a solid crystalline matrix of high temperature stability, a very unusual state of matter. Despite the weakness of the host-guest interactions, investigations on small crystallites of the HgX(2)-TON composites using a Raman microscope show a strong polarization dependence, providing evidence for an orientational alignment of the HgX(2) molecules inside the one-dimensional pore system of this host. For these reasons, the host matrices used in this study can be viewed as orienting solid solvents, coordinating only very weakly to the inserted HgX(2) guest molecules, but exhibiting a strong geometrical template function for their alignment. The concept of using electroneutral SiO(2) modifications as host components for a modular construction of new host-guest compounds thus allows the designed construction of ordered guest assemblies, with the pore systems of the rigid host matrices acting as space-confining and ordering templates for the guest components. 相似文献
133.
Thiocarbonylcompounds such as 1a, 1b, 1c, 1d, 1e and 1f were prepared and irradiated with UV- light in hexane solution. The products obtained in this photolyses are 3a, 3b and 3c. Only 3c dissociates in the temperature range 140-190° reversible to 2c. The others, 3a and 3b, decompose yielding bis(trifluoromethyl)diselenide, 6b and 6d, without forming the corresponding methyl radical 2a and 2b. This was proved by spin-trapping experiments utilizing phenyl-t-butylnitrone. Attempts to prepare 3e were unsuccessful but led to the new compounds 7a, 7b, 7c, 1,1,1-tris(trifluoromethylseleno)ethan (7d) and, surprisingly, 9. Physical and spectroscopic data of the newly prepared substances are provided. 相似文献
134.
Alois Smolka 《Monatshefte für Chemie / Chemical Monthly》1887,8(1):379-390
Ohne Zusammenfassung 相似文献
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136.
Dipl.‐Chem. Jens Willwacher Prof. Alois Fürstner 《Angewandte Chemie (International ed. in English)》2014,53(16):4217-4221
A concise synthesis of the putative structure assigned to the highly cytotoxic marine macrolide mandelalide A ( 1 ) is disclosed. Specifically, an iridium‐catalyzed two‐directional Krische allylation and a cobalt‐catalyzed carbonylative epoxide opening served as convenient entry points for the preparation of the major building blocks. The final stages feature the first implementation of terminal‐acetylene metathesis into natural product synthesis, which is remarkable as this class of substrates was beyond reach until very recently; key to success was the use of the highly selective molybdenum alkylidyne complex 42 as the catalyst. Although the constitution and stereochemistry of the synthetic samples are unambiguous, the spectra of 1 as well as of 11‐epi‐ 1 deviate from those of the natural product, which implies a subtle but deep‐seated error in the original structure assignment. 相似文献
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