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91.
Russian Journal of General Chemistry - Azomethines were synthesized from 2,4,6-trimethylaniline, salicylaldehyde, and its 3(5)-halogen derivatives, as well as their complexes with zinc(II) (ZnL2)....  相似文献   
92.
Russian Chemical Bulletin - The method of one-stage catalytic polycyclocondensation according to the B4 + AB scheme was used to synthesize new tetraarm star-shaped oligoimides (SOIs) with terminal...  相似文献   
93.
Russian Chemical Bulletin - Two new D—π—A chromophores with the tricyanofuranyl acceptor (A), an amphi-divinyl quinoxaline π-electron conjugated bridge, and the carbazole or...  相似文献   
94.
Synchrotron radiation-based Fourier transform infrared spectroscopy enables access to vibrational information from mid over far infrared to even terahertz domains. This information may prove critical for the elucidation of fundamental bio-molecular phenomena including folding-mediated innate host defence mechanisms. Antimicrobial peptides (AMPs) represent one of such phenomena. These are major effector molecules of the innate immune system, which favour attack on microbial membranes. AMPs recognise and bind to the membranes whereupon they assemble into pores or channels destabilising the membranes leading to cell death. However, specific molecular interactions responsible for antimicrobial activities have yet to be fully understood. Herein we probe such interactions by assessing molecular specific variations in the near-THz 400–40 cm−1 range for defined helical AMP templates in reconstituted phospholipid membranes. In particular, we show that a temperature-dependent spectroscopic analysis, supported by 2D correlative tools, provides direct evidence for the membrane-induced and folding-mediated activity of AMPs. The far-FTIR study offers a direct and information-rich probe of membrane-related antimicrobial interactions.  相似文献   
95.
Carbonized lignin has been proposed as a sustainable and domestic source of activated, amorphous, graphitic, and nanostructured carbon for many industrial applications as the structure can be tuned through processing conditions. However, the inherent variability of lignin and its complex physicochemical structure resulting from feedstock and pulping selection make the Process-Structure-Property-Performance (PSPP) relationships hard to define. In this work, radial distribution functions (RDFs) from synchrotron X-ray and neutron scattering of lignin-based carbon composites (LBCCs) are investigated using the Hierarchical Decomposition of the Radial Distribution Function (HDRDF) modelling method to characterize the local atomic environment and develop quantitative PSPP relationships. PSPP relationships for LBCCs defined by this work include crystallite size dependence on lignin feedstock as well as increasing crystalline volume fraction, nanoscale composite density, and crystallite size with increasing reduction temperature.  相似文献   
96.
Cellulose - In this work, we have developed methods of synthesis of cellulose nanocrystal (CNC) conjugates with chlorotriazine reactive dyes (RDs)—reactive violet, reactive-bright red and...  相似文献   
97.
Alkali-metal ferrates containing amide groups have emerged as regioselective bases capable of promoting Fe−H exchanges of aromatic substrates. Advancing this area of heterobimetallic chemistry, a new series of sodium ferrates is introduced incorporating the bulky arylsilyl amido ligand N(SiMe3)(Dipp) (Dipp=2,6-iPr2-C6H3). Influenced by the large steric demands imposed by this amide, transamination of [NaFe(HMDS)3] (HMDS=N(SiMe3)2) with an excess of HN(SiMe3)(Dipp) led to the isolation of heteroleptic [Na(HMDS)2Fe{N(SiMe3)Dipp}] ( 1 ) resulting from the exchange of just one HMDS group. An alternative co-complexation approach, combining the homometallic metal amides [NaN(SiMe3)Dipp] and [Fe{N(SiMe3)Dipp}2] induces lateral metallation of one Me arm from the SiMe3 group in the iron amide furnishing tetrameric [NaFe{N(SiCH2Me2)Dipp}{N(SiMe3)Dipp}]4 ( 2 ). Reactivity studies support that this deprotonation is driven by the steric incompatibility of the single metal amides rather than the basic capability of the sodium reagent. Displaying synergistic reactivity, heteroleptic sodium ferrate 1 can selectively promote ferration of pentafluorobenzene using one of its HMDS arms to give heterotrileptic [Na{N(SiMe3)Dipp}(HMDS)Fe(C6F5)] ( 4 ). Attempts to deprotonate less activated pyridine led to the isolation of NaHMDS and heteroleptic Fe(II) amide [(py)Fe{N(SiMe3)Dipp}(HMDS)] ( 5 ), resulting from an alternative redistribution process which is favoured by the Lewis donor ability of this substrate.  相似文献   
98.
Russian Chemical Bulletin - New potential biologically active derivatives, in which the sterically hindered pyrocatechol moiety is linked through a 2-thioacetyl covalent bridge to a number of...  相似文献   
99.
Russian Chemical Bulletin - The tandem Knoevenagel—Michael—intramolecular ammonolysis—alkylation reaction was used to synthesize functionalized tetrahydropyridones. The molecular...  相似文献   
100.
Russian Chemical Bulletin - The kinetic regularities of thermal destruction of polycarbonate films containing Pt, Au, Ag, and Ni nanoparticles were studied. Scanning and transmission electron...  相似文献   
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