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771.
Leimeng Zhuang Marcel Hoekman Willem Beeker Arne Leinse Ren Heideman Paulus van Dijk Chris Roeloffzen 《Laser \u0026amp; Photonics Reviews》2013,7(6):994-1002
In this paper, novel photonic delay lines (DLs) using Vernier/non‐identical ring resonators (VRRs) are proposed and demonstrated, which are capable of simultaneous generation of multiple different delays at different wavelengths (frequencies). The simple device architectures and full reconfigurability allow the DLs to be integrated with other functional building blocks in photonic integrated circuits to realize on‐chip, complex multi‐λ microwave photonic signal processors with reduced system complexity. To prove the concept, DLs using VRRs in cascaded and coupled configurations have been fabricated in TriPleXTM waveguide technology, which enables a very low delay‐induced loss of approximately 0.18 dB/100 ps. The fabricated DLs demonstrated simultaneous generation of four incremental delays, where a maximum incremental step of 550 ps and a corresponding top delay of 1650 ps were measured for a bandwidth up to 1 GHz. To our knowledge, this is the first report on VRRs for delay generation functionalities. 相似文献
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Arne Merschel Dr. Dennis Rottschäfer Beate Neumann Dr. Hans-Georg Stammler Dr. Mark Ringenberg Dr. Maurice van Gastel T. Ilgin Demirer Dr. Diego M. Andrada Priv.-Doz. Dr. Rajendra S. Ghadwal 《Angewandte Chemie (International ed. in English)》2023,62(5):e202215244
Herein, the first stable anions K[SIPrBp] ( 4 a-K ) and K[IPrBp] ( 4 b-K ) (SIPrBp=BpC{N(Dipp)CH2}2, IPrBp=BpC{N(Dipp)CH}2; Bp=4-PhC6H4; Dipp=2,6-iPr2C6H3) derived from classical N-heterocyclic carbenes (NHCs) (i.e. SIPr and IPr) have been isolated as violet crystalline solids. 4 a-K and 4 b-K are prepared by KC8 reduction of the neutral radicals [SIPrBp] ( 3 a ) and [IPrBp] ( 3 b ), respectively. The radicals 3 a and 3 b as well as [Me-IPrBp] 3 c (Me-IPrBp=BpC{N(Dipp)CMe}2) are accessible as crystalline solids on treatment of the respective 1,3-imidazoli(ni)um bromides (SIPrBp)Br ( 2 a ), (IPrBp)Br ( 2 b ), and (Me−IPrBp)Br ( 2 c ) with KC8. The cyclic voltammograms of 2 a–2 c exhibit two one-electron reversible redox processes in −0.5 to −2.5 V region that correspond to the radicals 3 a–3 c and the anions ( 4 a–4 c )−. Computational calculations suggest a closed-shell singlet ground state for ( 4 a–4 c )− with the singlet-triplet energy gap of 17–24 kcal mol−1. 相似文献
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Dr. Max Hohenschutz Dr. Pierre Bauduin Dr. Carlos G. Lopez Dr. Beate Förster Prof. Walter Richtering 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2023,135(3):e202210208
Nanometer-sized anions (nano-ions) like polyoxometalates and boron clusters exhibit so-called superchaotropic behavior, which describes their strong binding to hydrated non-ionic matter in water. We show here that nano-ions, at millimolar concentrations, dramatically enhance the viscosity and induce gelation of aqueous solutions of non-ionic cellulose ethers (CEs), a class of widely utilized polymers known for their thickening and gel-forming ability. These phenomena arise from an interplay of attractive forces and repulsive electrostatic forces between CE-chains upon nano-ion binding. The attractive forces manifest themselves as aggregation of CE-chains into a physically crosslinked polymer network (gel). In turn, the electrostatic repulsions hamper the viscosity increase and gelation. Superchaotropic nano-ion binding emerges as a novel and general physical crosslinking motif for CE-solutions and exceeds by far the conventional thickening effects of classical salts and ionic surfactants. 相似文献
775.
Dr. Niklas Aders Dr. Jan-Hendrik Lamm Katharina Wels Sophie Bernhardt Beate Neumann Dr. Hans-Georg Stammler Prof. Dr. Norbert W. Mitzel 《欧洲无机化学杂志》2023,26(17):e202300061
Herein we report the syntheses of highly rigid silicon- and tin-containing cyclic and bicyclic compounds with unsaturated organic backbones. The syntheses proceed via di-lithiated diethynylbenzene derivatives. The protocols for the known precursor compounds were significantly improved in a two-step one-pot reaction with yields up to 45 % by alternating addition of the lithiation reagent and starting material. A total of ten compounds were synthesized and the molecular structure in the solid state was elucidated for six novel compounds. Host-guest-experiments with selected molecules were conducted to investigate on the potential of the complexation of small anions. All compounds were characterized by multinuclear NMR spectroscopy and elemental analyses or mass spectrometry and in most parts by SC-XRD analyses. 相似文献
776.
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option. 相似文献
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J. Louis Beckmann Jonas Krieft Dr. Yury V. Vishnevskiy Beate Neumann Dr. Hans-Georg Stammler Prof. Dr. Norbert W. Mitzel 《Angewandte Chemie (International ed. in English)》2023,62(46):e202310439
A bidentate pnictogen bonding host-system based on 1,8-diethynylanthracene was synthesized by a selective tin-antimony exchange reaction and investigated regarding its ability to act as a Lewis acidic host component for the complexation of Lewis basic or anionic guests. In this work, the novel C≡C−Sb(C2F5)2 unit was established to study the potential of antimony(III) sites as representatives for the scarcely explored pnictogen bonding donors. The capability of this partly fluorinated host system was investigated towards halide anions (Cl−, Br−, I−), dimethyl chalcogenides Me2Y (Y=O, S, Se, Te), and nitrogen heterocycles (pyridine, pyrimidine). Insights into the adduct formation behavior as well as the bonding situation of such E⋅⋅⋅Sb−CF moieties were obtained in solution by means of NMR spectroscopy, in the solid state by X-ray diffraction, by elemental analyses, and by computational methods (DFT, QTAIM, IQA), respectively. 相似文献