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排序方式: 共有78条查询结果,搜索用时 15 毫秒
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Menozzi E Busi M Ramingo R Campagnolo M Geremia S Dalcanale E 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(10):3136-3148
The self-assembly of open ditopic and tetratopic cavitand complexes has been investigated by using monofunctionalized cavitand ligands and suitable metal precursors. In the case of ditopic complexes, self-assembly protocols, leading exclusively to the formation of both thermodynamically stable cis-Pt square-planar complexes 8 and 9 and the kinetically inert fac-Re octahedral complex 14, have been elaborated. The use of cis-[Pt(CH3)CN)2Cl2] as metal precursor led to the formation of monotopic trans-10 and ditopic trans-11 cavitand complexes, while cis-[Pt(dmso)2Cl2] afforded both cis-13 and trans-11 isomers. The self-assembly of tetratopic cavitand complexes has been achieved by using mononuclear [Pd(CH3CN)4(BF4)2] and dinuclear [M2(tppb)(OTf)4] (19: M = Pt; 20: M = Pd) metal precursors. Only the tetratopic dinuclear complexes 21 and 22 were stable. The ligand configuration with two phosphorus and two cavitand ligands at the metal centers is the most appropriate to build tetratopic cavitand complexes with sufficient kinetic stability. 相似文献
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Numerical Algorithms - In this paper, we propose and study the iteration complexity of an inexact Douglas-Rachford splitting (DRS) method and a Douglas-Rachford-Tseng’s forward-backward (F-B)... 相似文献
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We develop generalized bounds for quantum single-parameter estimation problems for which the coupling to the parameter is described by intrinsic multisystem interactions. For a Hamiltonian with k-system parameter-sensitive terms, the quantum limit scales as 1/Nk, where N is the number of systems. These quantum limits remain valid when the Hamiltonian is augmented by any parameter-independent interaction among the systems and when adaptive measurements via parameter-independent coupling to ancillas are allowed. 相似文献
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Tancini F Yebeutchou RM Pirondini L De Zorzi R Geremia S Scherman OA Dalcanale E 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(48):14313-14321
The outstanding complexing properties of tetraphosphonate cavitands towards N‐methylpyridinium salts were exploited to realise a new class of linear and cyclic AABB supramolecular polymers through host–guest interactions. The effectiveness of the selected self‐association processes was tested by 1H NMR studies, whereas microcalorimetric analyses clarified the binding thermodynamics and revealed the possibility of tuning entropic contributions by acting on the flexibility of the guest linker. Although the formation of linear polymeric chains for a rigid system was demonstrated by X‐ray analysis, the presence of a concentration‐dependent ring–chain equilibrium was indicated by solution viscosity measurements in the case of a very flexible ditopic BB guest co‐monomer. 相似文献
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CLAUDIA L. PARKER OSCAR N. VENTURA STAN K. BURT RAÚL E. CACHAU 《Molecular physics》2013,111(17):2659-2668
We present a general purpose QM-MM-MD engine (DYNGA) designed to test alternative hybrid Hamiltonians geared towards the treatment of problems of interest in structural biology including the use of experimental data constraints. In this first presentation we use DYNGA to explore the behaviour of a traditional QM-MM approach in the treatment of the water—water interaction. We find the potential energy hypersurface for the water dimer computed with the HF 4–31G*/TIP3P hybrid Hamiltonian tends to be too flat. We also explore the effect of using traditional QM-MM techniques on proton wires and conclude there is a need for improvement, possibly addressed by using polarizable force fields. 相似文献