SYNTHESIS AND CHARACTERIZATION OF DIAQUA(3-pTOLYLIMINO-2-BUTANONE OXIMATO)(3-p-TOLYLIMINO-2-BUTANONE OXIME)NICKEL(II) PERCHLORATE

Abstract

[Ni(L^?1)(HL)(H₂O)₂].ClO₄ with a Schiff base ligand L (HL = 3-p-tolylimino-2-butanone oxime) was prepared and structurally characterized by IR, cyclic voltammetry and X-ray diffraction methods. The nickel atom has distorted octahedral coordination consisting of four nitrogen atoms and two oxygen atoms. The equatorial plane is formed by two oxime nitrogen atoms and two imine nitrogen atoms of two Schiff base ligand (L^?1 and HL) with Ni‐ N bond distances between 2.01(1) and 2.11(1)Å. Water oxygen atoms occupy axial positions with Ni‐ O bond distances of 2.06(1) and 2.15(1) Å. The oxime groups in the Schiff base ligands are coordinated to Ni atom through their nitrogen atoms. One asymmetric intramolecular hydrogen bridge between the two oxime groups is found in the title complex.     

Nucleophilic addition of regioselectively lithiated indoline with aldimines for the syntheses of 2- and 7-indolinyl methanamine derivatives

Indolines bearing different N-protecting groups (N-Tbf and N-Boc) were deprotonated regioselectively at C-2 (sp³ hybridized ortho-H) and C-7 (sp² hybridized para-H) of the indoline ring, respectively. The generated organolithium intermediates reacted with aldimines to give the desired products in good yields with excellent anti-diastereoselectivities (>99:1). The produced N-Ts-(1-Tbf-indolin-2-yl)methanamine was facilely transformed to a fused heterocyclic compound.     

New imine compounds and their copper complexes: synthesis,characterization and comparative investigations of morphologic,mesomorphic, thermotropic,thermo-optical and thermodynamical properties

Investigations of the morphologic, mesomorphic, thermotropic, thermo-optical and thermodynamical properties of new imine compounds and their copper complexes, synthesized by our group, have been carried out. Temperature transformations of typical textures for mesophases, taking place in imine compounds and copper complexes, and the peculiarities of the biphasic regions at the direct and reverse mesophase–isotropic liquid and isotropic liquid–mesophase phase transitions have been investigated.     

Staudinger/aza-Wittig reactions utilizing a novel linear polymer-supported triphenylphosphine as a modified liquid-phase reagent

A new triphenylphosphine reagent linked to a linear maleimide-styrene copolymer is synthesized and is found to be effective for the formation of a variety of imines via the Staudinger/aza-Wittig reaction. This linear polymer-supported triphenylphosphine has a unique solubility behavior and provides for a simple means of purifying the desired imine from the phosphine oxide by-product. The reactivity of this polymeric reagent is superior to that of the cross-linked polymer-supported phosphine reagent.     

Transformation of Imine Cages into Hydrocarbon Cages

In contrast to organic cages which are formed by exploiting dynamic covalent chemistry, such as boronic ester cages, imine cages, or disulfide cages, those with a fully carbonaceous backbone are rarer. With the exception of alkyne metathesis based approaches, the vast majority of hydrocarbon cages need to be synthesized by kinetically controlled bond formation. This strategy implies a multiple step synthesis and no correction mechanism in the final macrocyclization step, both of which are responsible for low overall yields. Whereas for smaller cages the intrinsic drawbacks are not always obvious, larger cages are seldom synthesized in yields beyond a few tenths of a percent. Presented herein is a three‐step method to convert imine cages into hydrocarbon cages. The method has been successfully applied to even larger structures such as derivatives of C₇₂H₇₂ , an unknown cage suggested by Fritz Vögtle more than 20 years ago.     

Solvent-and Catalyst-free Synthesis and Antifungal Activities of α-Aminophosphonate Containing Cyclopropane Moiety

Nine new α-aminophosphonate derivatives containing cyclopropane moiety have been synthesized via conventional and microwave irradiation methods under solvent-and catalyst-free condition. The structures of the title compounds have been confirmed by 1H NMR, 31P NMR, FTIR, EI-MS and FTICR-MS. Their antifungal activities were evaluated in vivo and some of the compounds were found to exhibit excellent antifungal activities against Corynespora cassiicola, Pseudomonas syringae pv. Lachrymans, Pseudoperonospora cubensis and Sclerotinia sclerotiorum.     

Molecular Structure of Quinolin-1-(2-quinolyl)-2-one mesitylimine: An Unusual Amination Product of 2,4,6-Trimethylaniline and 2-Chloroquinoline

Abstract  The molecular structure of quinolin-1-(2-quinolyl)-2-one mesitylimine has been determined. The Buchwald-Hartwig amination of mesitylaniline with two equivalents of 2-chloroquinoline results in dearomatization of one quinoline heterocycle, forming an imine with the mesitylaniline nitrogen and aminating the second 2-chloroquinoline via the cyclic nitrogen. The mesityl and quinoline moieties are nearly perpendicular to the plane of the central quinolyl structure. Rationalization of the imine formation is found by a consideration of the relative stability of the syn and anti conformations of the reaction intermediate. Crystal data: space group P2₁/c, a = 12.609(3), b = 15.010(3), c = 12.456(3) ?, β = 112.68(3)°; V = 2,175.3(8) ?³, Z = 4, R = 0.0649, wR₂ = 0.1498. Graphical Abstract  The amination of mesitylaniline with two equivalents of 2-chloroquinoline results in dearomatization of one quinoline heterocycle, forming an imine with the mesitylaniline nitrogen and aminating the second 2-chloroquinoline via the cyclic nitrogen.      

Gold‐Catalyzed Synthesis of 1,3‐Diaminopyrazoles from 1‐Alkynyltriazenes and Imines

A new procedure for the synthesis of highly substituted 1,3‐diaminopyrazoles is described. As substrates, we have employed 1‐alkynyltriazenes and imines. The formation of pyrazoles was achieved by two‐fold C–N coupling reactions in the presence of (JohnPhos)AuCl and AgNT f₂ as catalyst precursors. The regioselectivity of the reaction was inferred from a crystallographic analysis of one reaction product.     

氨基二苯硒的酰化和缩合反应研究

４－氨基二苯硒分别与酸酐和醛进行酰化反应和缩合反应，合成了６种Ｎ－二苯硒胺羰基苯甲酸及１２个，Ｎ－二苯硒亚胺化合物，用元素分析，红外光谱，核磁共振谱表征了结构，结果表明在酰化反应和缩合反应中，４－氨基二苯硒与芳伯胺及氨基二茂铁的作用相同，产物结构类似，且均具有生物活性。