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991.
Frank Antonsen 《International Journal of Theoretical Physics》1998,37(2):697-757
We first introduce theWigner–Weyl–Moyal formalism for a theorywhose phase space is an arbitrary Lie algebra. We alsogeneralize to quantum Lie algebras and to supersymmetrictheories. It turns out that the noncommutativity leads to a deformation ofthe classical phase space: instead of being a vectorspace, it becomes a manifold, the topology of which isgiven by the commutator relations. It is shown in fact that the classical phase space, for asemisimple Lie algebra, becomes a homogeneous symplecticmanifold. The symplectic product is also deformed. Wefinally make some comments on how to generalise to C*-algebras and other operator algebras,too. 相似文献
992.
Alejandro Cervantes-Reyes Dr. Frank Rominger Prof. Dr. A. Stephen K. Hashmi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(24):5530-5540
The synthesis and full characterization of new air-stable AgI and CuI complexes bearing structurally bulky expanded-ring N-heterocyclic carbene (erNHC) ligands is presented. The condensation of protonated NHC salts with Ag2O afforded a collection of AgI complexes, and their first use as ligand transfer reagents led to novel isostructural CuI or AuI complexes. In situ deprotonation of the NHC salts in the presence of a copper(I) source, provides a library of new CuI complexes. The solid-state structures feature large N-CNHC-N angles (118–128°) and almost identical angles between the aryl groups on the nitrogen atoms and the plane of the N-C-N unit of the carbene (i.e. torsion angles close to 0°). Among the steric parameters, the percent buried volume (%Vbur) values span easily in the 50–57 % range, and that one of (9-Dipp)CuBr complex (%Vbur=57.5) overcomes to other known erNHC–metal complexes reported to date. Preliminary catalytic experiments in the copper-catalyzed coupling between N-tosylhydrazone and phenylacetylene, afforded 76–93 % product at the 0.5–2.5 mol % catalyst loading, proving the stability of CuI erNHC complexes at elevated temperatures (100 °C). 相似文献
993.
Jean-Noël Marsat Frank Stahlhut André Laschewsky Hans v. Berlepsch Christoph Böttcher 《Colloid and polymer science》2013,291(11):2561-2567
An amphiphilic linear ternary block copolymer was synthesised in three consecutive steps via reversible addition–fragmentation chain transfer polymerisation. Oligo(ethylene glycol) monomethyl ether acrylate was engaged as a hydrophilic building block, while benzyl acrylate and 3-tris(trimethylsiloxy)silyl propyl acrylate served as hydrophobic building blocks. The resulting “triphilic” copolymer consists thus of a hydrophilic (A) and two mutually incompatible “soft” hydrophobic blocks, namely, a lipophilic (B) and a silicone-based (C) block, with all blocks having glass transition temperatures well below 0 °C. The triphilic copolymer self-assembles into spherical multicompartment micellar aggregates in aqueous solution, where the two hydrophobic blocks undergo local phase separation into various ultrastructures as evidenced by cryogenic transmission electron microscopy. Thus, a silicone-based polymer block can replace the hitherto typically employed fluorocarbon-based hydrophobic blocks in triphilic block copolymers for inducing multicompartmentalisation. 相似文献
994.
995.
We show that NIP fields have no Artin-Schreier extension, and that simple fields have only a finite number of them. 相似文献
996.
Xiong C Zhang J Davis P Wang W Ying J Porreca F Hruby VJ 《Chemical communications (Cambridge, England)》2003,(13):1598-1599
Novel constrained beta-turn dipeptide mimetics, 8-phenyl thiaindolizidinone amino acids 3, have been synthesized stereoselectively and incorporated into Leu-enkephalin peptides as a replacement of dipeptide Gly3-Phe4 to afford four individual isomers of Leu-enkephalin analogues 6. 相似文献
997.
998.
Werner Uhl Frank Hengesbach Jennifer Isermann Meisam Soleimani Lina Schürmann Alexander Hepp Marcus Layh 《无机化学与普通化学杂志》2019,645(20):1205-1214
Hydrogallation of Me3Si–C≡C–NR'2 with R2Ga–H (R = tBu, CH2tBu, iBu) yielded Ga/N‐based active Lewis pairs, R2Ga–C(SiMe3)=C(H)–NR'2 ( 7 ). The Ga and N atoms adopt cis‐positions at the C=C bonds and show weak Ga–N interactions. tBu2GaH and Me3Si–C≡C–N(C2H4)2NMe afforded under exposure of daylight the trifunctional digallium(II) compound [MeN(C2H4)2N](H)C=C(SiMe3)Ga(tBu)–Ga(tBu)C(SiMe3)=C(H)[N(C2H4)2NMe] ( 8 ), which results from elimination of isobutene and H2 and Ga–Ga bond formation. 8 was selectively obtained from the ynamine and [tBu(H)Ga–Ga(H)tBu]2[HGatBu2]2. 7a (R = tBu; NR'2 = 2,6‐Me2NC5H8) and H8C4N–C≡N afforded the adduct tBu2Ga‐C(SiMe3)=C(H)(2,6‐Me2NC5H8) · N≡C–NC4H8 ( 11 ) with the nitrile bound to gallium. The analogous ALP with harder Al atoms yielded an adduct of the nitrile dimer or oligomers of the nitrile at room temperature. The reaction of 7a with Ph–N=C=O led to the insertion of two NCO groups into the Ga–Cvinyl bond to yield a GaOCNCN heterocycle with Ga bound to O and N atoms ( 12 ). 相似文献
999.
The accuracy of instrumental neutron activation analysis is dependent upon measurement of the neutron flux to which samples are submitted. Flux monitoring techniques described and evaluated include: target cooling water activity, BFa counters, plastic scintillators, and a simple reference sample system. Evaluation is made on the basis of results obtained for oxygen analysis using primary standard materials. The superiority of the reference sample system for flux measurement during irregular neutron flux production is shown. 相似文献
1000.
Norbert Moszner Juraj Pavlinec Iris Lamparth Frank Zeuner Jrg Angermann 《Macromolecular rapid communications》2006,27(14):1115-1120
Summary: 1,3‐Bis(methacrylamido)propane‐2‐yl dihydrogen phosphate ( 1 ) was synthesised by phosphorylation of 1,3‐bis(methacrylamido)‐2‐hydroxypropane ( 2 ) with phosphorus oxychloride in tetrahydrofuran (THF) in the presence of triethylamine (TEA). The structure of the new monomer 1 was characterised by IR, 1H NMR, 13C NMR and 31P NMR spectroscopies, elemental analysis and mass spectrometry. The monomer dissolves well in water, ethanol or aqueous THF and shows an improved hydrolytic stability compared to the corresponding methacrylate‐based dihydrogen phosphates. 1 was homopolymerised in ethanol with 2,2′‐azoisobutyronitrile (AIBN) as the initiator at 55–75 °C under the formation of an insoluble, cross‐linked product. Aqueous solutions of 1 are strongly acidic and enable to etch enamel and dentin. Nevertheless, 1 did not show any cytotoxic effect. Furthermore, the adhesive properties of 1 were measured.