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31.
Gerd Becker Winfried Becker Gudrun Uhl Werner Uhl Hans-Jürgen Wessely 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-3):7-10
Abstract Alkyl- or arylbis(trimethylsilyl)phosphines as well as tris(trimethylsilyl)phosphine and the corresponding arsines react with acyl chlorides to give [1-(trimethylsiloxy)alkylidene]phosphines 1 and -arsines 2; most of their 2,2-dimethylpropylidene derivatives are thermally stable at room temperature. With the same class of phosphines as starting compounds and carbon disulfide [bis(trimethylsilylsulfano)methylidene]phosphines 3 are formed, whereas [(dialkylamino)methylidene]-4 and [diarylmethylidene]phosphines 5 or the corresponding arsines 6 and 7 can be obtained from acyl amides or ketones.1 相似文献
32.
Daniel Vogler Maximilian Schöner Dr. Elisabeth Kaifer Prof. Dr. Dr. Hans-Jörg Himmel 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(49):e202201389
In this work we report the first cycloaddition reactions between a diazido diborane(4) and terminal alkynes, providing unique access to bis-1,2,3-triazoles connected by a B−B bridge. The catalyst-free reactions are highly selective, yielding exclusively the thermodynamically disfavored bis-1,4-triazoles. The reactions are enabled by the high thermal stability of the diazido-diborane [B(hpp)(N3)]2 (hpp=1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-α]pyrimidinate). Due to the tetra-coordinate boron atoms in this reagent, the reactions are tolerant with respect to the introduction of Lewis-basic groups at the alkyne. The scope and limitations of the new reactions are discussed. 相似文献
33.
Lukas Lohmeyer Marco Werr Dr. Elisabeth Kaifer Prof. Hans-Jörg Himmel 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(60):e202201789
The field of molecular transition metal complexes with redox-active ligands is dominated by compounds with one or two units of the same redox-active ligand; complexes in which different redox-active ligands are bound to the same metal are uncommon. This work reports the first molecular coordination compounds in which redox-active bisguanidine or urea azine (biguanidine) ligands as well as oxolene ligands are bound to the same cobalt atom. The combination of two different redox-active ligands leads to mono- as well as unprecedented dinuclear cobalt complexes, being multiple (four or six) center redox systems with intriguing electronic structures, all exhibiting radical ligands. By changing the redox potential of the ligands through derivatisation, the electronic structure of the complexes could be altered in a rational way. 相似文献
34.
René Stangenberg Christos Grigoriadis Hans-Jürgen Butt Klaus Müllen George Floudas 《Colloid and polymer science》2014,292(8):1939-1948
The thermodynamic, optical, structural, and dynamic properties of the semifluorinated (E)-1-(4-octylphenyl)-2-(4-(perfluorooctyl)phenyl)diazene (4) and the corresponding (E)-1,2-bis(4-octylphenyl)diazene (5) have been studied with differential scanning calorimetry, polarizing optical microscopy, X-ray diffraction, and dielectric spectroscopy. 4 combines the azobenzene properties with the fluorophobic effect and gives rise to a responsive material with a temperature and dc-bias-driven switchable dielectric permittivity within the narrower nematic phase. This is caused by the nematic potential that inevitably brings some fluorocarbon chains in proximity to the hydrocarbon chains from adjacent molecules. Frustration is alleviated by reducing the nematic-to-isotropic transition temperature and by increasing the crystalline-to-nematic transition temperature, thus limiting the stability of the nematic phase. Unlike the normal isotropic phase of compound 5, the isotropic phase of compound 4 contains dipoles with short-range orientation correlations. Optimizing the type of interactions may result in materials with applications as molecular switches and electrooptic devices. 相似文献
35.
The new scandium(III) carbodiimides Sc2(CN2)3 and Sc2O2(CN2) were prepared by solid-state metathesis reactions between Li2(CN2) and ScCl3 and, regarding Sc2O2(CN2), Sc2O3 was added. The X-ray powder diffraction pattern refinements lead to a trigonal-rhombohedral (R3 c) crystal system for Sc2(CN2)3 and to an orthorhombic (Immm) crystal system for Sc2O2(CN2). The structure of Sc2(CN2)3 is isotypic to the well-known rare earth carbodiimides RE2(CN2)3 with the smaller cations RE = Tm, Yb, and Lu, whereas Sc2O2(CN2) is not isotypic to the known RE2O2(CN2) (RE = Y, La, Ce–Gd, except Pm) compounds. Both crystal structures are represented by layered arrangements of scandium, respectively scandium and oxide, alternating with carbodiimide layers. 相似文献
36.
Daniel Leibig Margarita Messerle Tobias Johann Christian Moers Farzaneh Kaveh Hans-Jürgen Butt Doris Vollmer Axel H. E. Müller Holger Frey 《Journal of polymer science. Part A, Polymer chemistry》2020,58(1):181-192
Well-defined polystyrene homopolymers with surface-adhesive triethoxysilyl end group were synthesized via living carbanionic polymerization, epoxide end-functionalization and subsequent hydrosilylation with triethoxysilane. Grafting-to performance of polymers with various molecular weight (Mn = 3000–14,000 g mol−1) to a silicon surface was examined in dependence of reaction time, polymer concentration, solvent and number of alkoxysilyl end groups. Crosslinkable polymers for surface modification were synthesized by statistical carbanionic copolymerization of 4-vinylbenzocyclobutene (4-VBCB) and styrene, followed by epoxide end-functionalization and triethoxysilane modification (Mn = 4000–14,000 g mol−1). The copolymers were characterized by 1H-NMR, THF-SEC, and matrix-assisted laser desorption and ionization time-of-flight mass spectrometry. In situ 1H-NMR kinetic studies in cyclohexane-d12 provided information regarding the monomer gradient in the polymer chains, with styrene being the more reactive monomer (rs = 2.75, r4-VBCB = 0.23). Thin polymer films on silicon wafers were prepared by grafting-to surface modification under conditions derived for the polystyrene homopolymer. The traceless, thermally induced crosslinking reaction of the benzocyclobutene units was studied by DSC in bulk as well as in 3–6 nm thick polymer films. Crosslinked films were analyzed by atomic force microscopy, ellipsometry, and nanoindentation, showing smooth polymer films with an increased modulus. © 2019 The Authors. Journal of Polymer Science published by Wiley Periodicals, Inc. J. Polym. Sci. 2020 , 58, 181–192 相似文献
37.
Kaliyamoorthy Panneerselvam Kizakkekoikkal K. Chacko Edwin Weber Hans-Jürgen Kühler 《Journal of inclusion phenomena and macrocyclic chemistry》1990,9(4):337-347
Single crystal X-ray analysis of a 1 : 2 complex between the dinaphthopyridino-l8-crown-6 host (1) and acetonitrile is reported. Crystals of the complex are monoclinic,P21/c witha = 12.178(5),b = 8.186(1),c = 30.873(1) Å, = 96.86(1)°, andD
c = 1.25 g cm–3 forZ = 4. The host molecule reveals an approximate mirror symmetry and exists in a so-called dentist's chair conformation. One of the acetonitrile guest molecules is involved in possible weak interactions to two oxygen atoms of the host macroring, while the other fills free lattice space only. 相似文献
38.
Mathematische Annalen - 相似文献
39.
Hans-Jörg Reiffen 《Mathematische Annalen》1966,164(3):272-279
Ohne Zusammenfassung 相似文献
40.
Let k be a commutative ring, GG finite affine algebraic k-groups, and HH the dual Hopfalgebras of the affine algebras of G resp. G. The main results of this paper are: (I) If k is semilocal (e.g. k a field) there is an H-linear, HH-colinear, unitary, augmented isomorphism HHH H, where HH is the coalgebra belonging to G/G. (II) If the k-submodule of the fixelements of (HH)* is isomorphic to k (e.g. k principal or semilocal), then HH is a Frobeniusextension of the second kind. 相似文献