Synthesis and solid-state structural characterisation of Pt(II,IV) bromide complexes containing bidentate organothiomethylpyridine heteroleptic ligands

A convenient synthetic method for the preparation of organothiomethylpyridine ligands 2-(RSCH₂)C₅H₄N (R = Ph (L¹), Me (L²)), 2-MeS–6-Me-C₅H₃N (L³), and 2-MeS–4-Me-C₅H₃N (L⁴) via the initial lithiation of substituted 2-picolines followed by the nucleophilic reaction with a diorganyldisulfide is described. The complexes [PtBr₂L] (L = L¹–L⁴) have been prepared in good to high yields as yellow solids with low solubility in organic solvents. The solid state structures of the complexes have been determined, showing the spatial arrangement of the complexes to depend significantly upon varying substituents within the ligand. The complexes undergo oxidation by bromine to form the tetravalent complexes [PtBr₄(L)] (L = L¹–L⁴). The solid state structures of [PtBr₄(L²)] and [PtBr₄(L₄)] have been determined, and shown to be monomeric with the ligand chelating the platinum centre.     

手性胺膦配体在不对称催化中的应用

利用邻二苯基膦苯甲醛分别与多种手性二胺的缩合反应,设计合成了一系列新型手性四齿胺膦配体.这类多齿胺膦配体含有两个软的磷原子和两个硬的氮原子,具有丰富的配位化学性能和优秀的不对称诱导能力.本文综述了手性胺膦金属络合物催化剂在不对称转移氢化反应、氧化动力学拆分反应、烯烃的不对称环氧化反应和不对称环丙烷化反应、不对称D-A反应中的应用.     

Molecular organization in MAPLE‐deposited conjugated polymer thin films and the implications for carrier transport characteristics

The morphological structure of poly(3‐hexylthiophene) (P3HT) thin films deposited by both Matrix Assisted Pulsed Laser Evaporation (MAPLE) and solution spin‐casting methods are investigated. The MAPLE samples possessed a higher degree of disorder, with random orientations of polymer crystallites along the side‐chain stacking, π–π stacking, and conjugated backbone directions. Moreover, the average molecular orientations and relative degrees of crystallinity of MAPLE‐deposited polymer films are insensitive to the chemistries of the substrates onto which they were deposited; this is in stark contrast to the films prepared by the conventional spin‐casting technique. Despite the seemingly unfavorable molecular orientations and the highly disordered morphologies, the in‐plane charge carrier transport characteristics of the MAPLE samples are comparable to those of spin‐cast samples, exhibiting similar transport activation energies (56 vs. 54 meV) to those reported in the literature for high mobility polymers. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2017 , 55, 39–48     

High selectively oxidative bromination of toluene derivatives by the H_2O_2-HBr system

An aqueous solution of hydrogen peroxide and hydrogen bromide illuminated by a 60 W incandescent light bulb serves as a source of bromine radicals.Various substituted toluenes（NO₂,Cl,Br,H,CH₃） were high selectively brominated at the benzyl position for monobromination in CH₂C1₂ at ice water with catalyst free.This simple but effective bromination of toluene derivatives with an aqueous H₂O₂-HBr system is characterized with the use of inexpensive reagents and a lower impact on the environment, which make it a good alternative to the existing bromination methods.     

The Effect of Alcohol and Carbonyl Functional Groups on the Competition between Unimolecular Decomposition and Isomerization in C4 and C5 Alkoxy Radicals

Presented here are computed rates for the thermal unimolecular decomposition of a variety of alkoxy radicals with four‐ and five‐carbon length backbones. Three classes of molecules are examined: alkoxy radicals with saturated hydrocarbon backbones, those with alcohol functional groups, and those with carbonyl functional groups. The chosen species represent many of those found during the combustion of fossil fuels as well as bio‐derived alternatives. Density functional theory calculations were benchmarked against higher level coupled cluster calculations and used to explore the potential energy surfaces of these systems. Transition state theory was used to calculate high‐pressure limit rate coefficients of all radical intermediates in the regimes relevant to atmospheric chemistry and combustion. We show that the assumption that alkoxy radicals quickly decompose via β‐scission to aldehydes and other radicals is not valid for some of the alkoxy radicals investigated in this work. We further illustrate how intra‐H migrations in larger alkoxy radicals with carbonyl and alcohol functional groups can dominate unimolecular decomposition under combustion and atmospheric relevant conditions. Finally, we discuss why carbonyl groups can increase or decrease intra‐H migration barriers depending on their location relative to the transferring H‐atom.     

A New Generation of Smart Amine Donors for Transaminase‐Mediated Biotransformations

The application of ω‐transaminase biocatalysts for the synthesis of optically pure chiral amines presents a number of challenges, including difficulties associated with displacing the challenging reaction equilibria. Herein, we report a highly effective approach using low equivalents of the new diamine donor, cadaverine, which enables high conversions of challenging substrates to the corresponding chiral amines in excellent ee. This approach paves the way for the design of self‐sufficient fermentation processes combining transaminase biotransformations with existing strategies for cadaverine production by decarboxylation of endogenous lysine.     

On 321-Avoiding Permutations in Affine Weyl Groups

We introduce the notion of 321-avoiding permutations in the affine Weyl group W of type A _{n – 1} by considering the group as a George group (in the sense of Eriksson and Eriksson). This enables us to generalize a result of Billey, Jockusch and Stanley to show that the 321-avoiding permutations in W coincide with the set of fully commutative elements; in other words, any two reduced expressions for a 321-avoiding element of W (considered as a Coxeter group) may be obtained from each other by repeated applications of short braid relations.Using Shi's characterization of the Kazhdan–Lusztig cells in the group W, we use our main result to show that the fully commutative elements of W form a union of Kazhdan–Lusztig cells. This phenomenon has been studied by the author and J. Losonczy for finite Coxeter groups, and is interesting partly because it allows certain structure constants for the Kazhdan–Lusztig basis of the associated Hecke algebra to be computed combinatorially.We also show how some of our results can be generalized to a larger group of permutations, the extended affine Weyl group associated to GL _n ()