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1.
N-Mono and N,N-disubstituted selenoamides are synthesized in a one-pot procedure from nitriles, selenium metal and NaBH4 followed by the amine group exchange of the intermediate primary selenoamide with an amine. 相似文献
2.
R. R. Khairullina B. F. Akmanov T. V. Tyumkina R. V. Kunakova A. G. Ibragimov 《Russian Journal of Organic Chemistry》2012,48(2):175-179
Efficient method was developed for thiols aminomethylation using N,N,N′,N′-tetra-methylmethanediamine in the presence of Sm and Fe salts. Aminosulfides were obtained in high yields and selectivity. 相似文献
3.
Tiina Maaninen Heikki M. Tuononen Katja Kosunen Raija Oilunkaniemi Johanna Hiitola Risto Laitinen Tristram Chivers 《无机化学与普通化学杂志》2004,630(12):1947-1954
Supermesityl selenium diimide [Se{N(C6H2tBu3‐2, 4, 6)}2; Se{N(mes*)}2] can be prepared in a good yield from the reaction of SeCl4 and (mes*)NHLi. The molecule adopts an unprecedented anti, anti‐conformation, as deduced by DFT calculations at PBE0/TZVP level of theory and supported by 77Se NMR spectroscopy and a crystal structure determination. An analogous reaction involving (C6H2Me3‐2, 4, 6)NHLi [(mes)NHLi] unexpectedly lead to the reduction of selenium and afforded the selenium diamide Se{NH(mes)}2 that was characterized by X‐ray crystallography and 77Se NMR spectroscopy. The Se‐N bonds of 1.847(3) and 1.852(3) Å show normal single bond lengths. The <NSeN bond angle of 109.9(1)° also indicates a tetrahedral AX2E2 bonding arrangement around selenium. Two N‐H···N hydrogen bonds link the Se{NH(mes)}2 molecule with two discrete (mes)NH2 molecules. In the solid state selenium diamide adopts the anti‐conformation, whereas in solution the presence of both syn‐ and anti‐isomers could be observed. PBE0/TZVP calculations of the shielding tensors of 28 different types of selenium‐containing molecules, for which the 77Se chemical shifts are unambiguously known, were carried out to assist the spectral assignment of Se{N(mes*)}2 and Se{NH(mes)}2. 相似文献
4.
N,N,N′,N′‐tetraalkyaminoazoxybenzene derivatives were conveniently prepared by the coupling of N,N‐dialkylnitrosoaniline in the presence of acetone and KOH. The reaction mechanism was proposed and investigated, and the structure of compound 3b was also confirmed by single crystal X‐ray diffractometry. 相似文献
5.
Navjeet Kaur 《合成通讯》2013,43(15):1711-1742
The development of new strategies for the synthesis of small-sized heterocycles has remained a highly attractive but challenging proposition. An overview of the application of microwave irradiation to the synthesis of five-membered heterocyclic compounds containing three and four nitrogen atoms is presented, focusing on the developments in the past 5–10 years. This contribution covers the literature concerning the total synthesis of N,N,N- and N,N,N,N-heterocycles. The literature data are summarized based on the size and type of cycles. 相似文献
6.
Zinc Complexes of a New N, N, O Ligand The tridentate ligand N, N(2‐dimethylaminoethyl)‐3, 5‐di‐tert.‐butyl‐salicylaldimine ( L H) results from the corresponding salicylic aldehyde and N, N‐dimethyl ethylenediamine. With zinc salts it forms the mononuclear halide complexes [ L ZnCl ˙ CH3OH] ( 1 ) and [ L ZnI ˙ CH3OH] ( 2 ) and the presumably polymeric acetate [ L ZnOCOCH3] ( 3 ). With diethyl zinc and diphenylphosphoric acid it yields the phosphate complex [ L Zn‐OPO(OPh)2 ˙ CH3OH] ( 4 ). The coordination of the complexes, which is between trigonal bipyramidal and square pyramidal, and the character of the five donors in the phosphate complex represent the transition state of a hydrolytic substrate cleavage in a zinc enzyme. 相似文献
7.
Dimitri Matioszek Oleksii Brusylovets D. James Wilson Stéphane Mazières Mathias Destarac 《Journal of polymer science. Part A, Polymer chemistry》2013,51(20):4361-4368
A new range of selenium‐based reversible addition‐fragmentation chain‐transfer (RAFT) agents is described and tested in the polymerization of styrene, acrylates, vinyl esters, and N‐vinylcaprolactam. The synthesized N,N‐dimethyldiselenocarbamates were poor control agents for styrene polymerization, whereas polyacrylates of controlled molar masses and bearing a diselenocarbamate terminal group could be synthesized. The polymerization of vinyl acetate and vinyl pivalate proceeded in a controlled manner as confirmed by size‐exclusion chromatography, matrix‐assisted laser desorption ionization‐time‐of‐flight mass spectrometry, and 77Se NMR analyses. The capability of these RAFT agents to control the polymerization of both more‐activated monomers and less‐activated monomers was exemplified through the synthesis of a poly(t‐butyl acrylate)‐b‐poly(vinyl acetate) diblock copolymer. Considering the very broad range of carbamate groups which can be envisioned, this finding opens numerous perspectives for diselenocarbamate‐mediated RAFT polymerization with its specificities yet to be explored. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 4361–4368 相似文献
8.
The Crystal Structure of Tris(N,N-diethyl-N′-benzoylselenoureato)cobalt(III) Co(C12H15N2OSe)3 crystallizes in the trigonal space group P3 . The cell parameters are a = 16.697(4), c = 8.557(8) Å, Z = 2. The structure was solved with Patterson and direct methods and was refined to a final R-value of 4.59%. CoIII is bidentally coordinated to three N,N-diethyl-N′-benzoylselenourea molecules to form a distorted octahedron with facial arrangement of the selenium and oxygen donor atoms. The Co? Se and Co? O bond lengths are 2.328(2) and 1.943(6) Å, respectively. The arrangement of the molecules within the unit cell leads to the formation of hexagonal channels parallel to the crystallographic c-axis. The wall of the channels is formed by carbon atoms of the phenyl group. The diameter of the channels is 8.148 Å. 相似文献
9.
Yu. V. Shulevich T. Kh. Nguen A. V. Navrotskii I. A. Novakov 《Russian Journal of Applied Chemistry》2009,82(9):1582-1586
Possibility of using complexes based on poly-N,N,N,N-trimethyl[methacryloyloxyethyl]ammonium methyl sulfate and sodium dodecyl sulfate for purification of fat-containing wastewater
was examined. 相似文献
10.
M. Drobni
-Koorok S. Polanc B. Stanovnik M. Tiler B. Ver
ek 《Journal of heterocyclic chemistry》1978,15(7):1105-1112
The free energies of the rotational barriers, ΔG*, about ?CH? NMe2 bond in N′-heteroaryl N,N-dimethylformamidines (A), about ?CH? NEt2 bond in N-heteroaryl N,N-diethylformamidines (B), and about ?C(Me)? NMe2 bond in N′-heteroaryl N,N-dimethylacetamidines (C) have been found to be in the range 17.5–20.1 kcal/mole for type A, 18.8–21.6 kcal/mole for type B and 13–14 kcal/mole or below for type C of compounds, respectively. The compounds of the types A and B exist in the forms IIa, IIIa, IV, V, and VI, while the compounds of the type C exist in the forms IIb and IIIb. 相似文献
11.
Eike Gellermann Uwe Klingebiel Thomas Pape Fabio Dall Antonia Thomas R. Schneider Stefan Schmatz 《无机化学与普通化学杂志》2001,627(12):2581-2588
Silylhydrazines and Dimeric N,N′‐Dilithium‐N,N′‐bis(silyl)hydrazides – Syntheses, Reactions, Isomerisations Di‐tert.‐butylchlorosilane reacts with dilithiated hydrazine in a molar ratio to give the N,N′‐bis(silyl)hydrazine, [(Me3C)2SiHNH]2, ( 5 ). Isomeric tris(silyl)hydrazines, N‐difluorophenylsilyl‐N′,N′‐bis(dimethylphenylsilyl)hydrazine ( 7 ) and N‐difluorophenylsilyl‐N,N′‐bis(dimethylphenylsilyl)hydrazine ( 8 ) are formed in the reaction of N‐lithium‐N′‐N′‐bis(dimethylphenylsilyl)hydrazide and F3SiPh. Isomeric bis(silyl)hydrazines, (Me3C)2SiFNHNHSiMe2Ph ( 9 ) and (Me3C)2‐ SiF(PhMe2Si)N–NH2 ( 10 ) are the result of the reaction of di‐tert.‐butylfluorosilylhydrazine and ClSiMe2Ph in the presence of Et3N. Quantum chemical calculations for model compounds demonstrate the dyotropic course of the rearrangement. The monolithium derivative of 5 forms a N‐lithium‐N′,N′‐bis(silyl)hydrazide ( 11 ). The dilithium salts of 5 ( 13 ) and of the bis(tert.‐butyldiphenylsilyl)hydrazine ( 12 ) crystallize as dimers with formation of a central Li4N4 unit. The formation of 12 from 11 occurs via a N′ → N‐silyl group migration. Results of crystal structure analyses are reported. 相似文献
12.
《化学:亚洲杂志》2017,12(17):2237-2244
A general approach to the synthesis of borohydride complexes containing one or two dinitroamide fragments has been suggested. Based on a smooth substitution of halide in haloborane or dibromoborane complexes with N ,N ‐dinitroamide salts, this method provides various N ,N ‐dinitroamidoboranes complexes in good yields and in analytically pure form. By means of spectroscopic and computational methods, it was demonstrated that dinitroamidoborane complexes could form as both B,N‐ and B,O‐isomers, which did not interconvert at ambient temperature. 相似文献
13.
Valentina K. Yu Tynyshtyk K. Iskakova Marat F. Faskhutdinov Kaldybay D. Praliyev Chengeer P. Lee 《Phosphorus, sulfur, and silicon and the related elements》2014,189(7-8):864-872
AbstractBased upon the analysis of 1H NMR data, along with molecular modeling, it was shown that the reduction of 3,7-dihetera(N,N-; N,O-; N,S-)bicyclo[3.3.1]nonan-9-ones by LiAlH4 led to a mixture of two stereoisomeric secondary alcohols with different orientations of the hydroxyl groups in one of the ring systems. Diaza derivatives in deuterochloroform exist in predominant chair-boat conformations. However, the replacement of nitrogen in one of the heterocycles by oxygen or sulfur led to stereoisomers one of which existed in chair-boat conformation and another in a chair–chair conformation. In all cases the boat conformation is stabilized by formation of an intramolecular hydrogen bond (IMHB) between a lone electron pair of the nitrogen atom and a proton on the pseudo axial hydroxyl group of the other ring. 相似文献
14.
N, N, N′,N′-Tetrabutyl-3,6-dioxaoctan-dithioamid, an Ionophore with Cd2+-Selectivity The CdCl2-complex of N, N, N′, N′-tetrabutyl-3, 6-dioxaoctanedithioamide crystallizes with the composition [Ligand. Cd2Cl4] in space group P1 , a= 14.140, b= 10.025, c= 12.173 Å, α = 95.59°. β = 102.06°. γ = 85.50° Z= 2. Each ligand coordinates two Cd2+-ions. Adjacent cations are bridged by two Cl+-ions such that infinite bands along the b-axis are formed. 相似文献
15.
Ahmed O. Maslat Ibrahim Jibril Mahmoud Abussaud Emad H. Abd‐Alhadi Zuhair Hamadah 《应用有机金属化学》2002,16(1):44-50
A new series of bifunctional organoiron thio‐ and seleno‐terephthalate complexes — (η‐C5H5)Fe(CO)2ECO(C6H4)COX [E = S; X = C6H11NH, (C2H5)2N; and E = Se; X = P? CH3? C6H4? NH, C6H5? C2N2O? S, m? NO2? C6H4? CH?CH? COO] — has been synthesized via the organic transformation reactions of the terephthaloyl chloride precursors η‐(C5H5)Fe(CO)2ECO(C6H4)COCl with the desired nucleophiles. These new complexes were characterized by elemental analysis, IR and 1H NMR spectra. The above complexes, in addition to some other selected analogues, were tested for their antifungal, antibacterial and mutagenic activity. Our results show that all the selenium‐containing compounds have antifungal activity on Candida albicans and antibacterial effects against Bacillus subtilis and Staphylococcus aureus. Four of the six selenium‐containing derivatives exhibited growth inhibitory effects against Pseudomonas aeruginosa and/or Escherichia coli. Sulfur‐containing derivatives elicited activity against C. albicans, and each one of them showed activity against at least one of the bacterial strains that have been used in this investigation. Two selenium‐ and two sulfur‐containing derivatives showed mutagenic activity against one or more than one strain of the Salmonella typhimurium using the Ames test. Copyright © 2001 John Wiley & Sons, Ltd. 相似文献
16.
Niyazi Biak Bahire Filiz enkal Tuba imanolu Cemal
zerolu 《Journal of polymer science. Part A, Polymer chemistry》2000,38(6):1006-1013
N,N,N′,N′‐tetraallyl piperazinium dibromide (TAP) has been prepared in high yields by quaternization of N,N′‐diallyl piperazine with allyl bromide. Herein, we have described preparation of nonhydrolysable, strong, cationic hydrogels by copolymerization of TAP with N,N‐diallyl morpholinium bromide (DAM) in the presence of t‐butyl hydroperoxide as initiator in aqueous solutions. Because the monomer and crosslinker involved consist of quaternary amine functions, these hydrogels are fully cationic and do not carry hydrolysable groups. Contrary to expectations, the quaternary amine hydrogels presented do not show any super absorbency, instead dry gel particles in water undergo spontaneous disintegration with an audible bursting of the particles due to instantaneous, high osmotic pressure. Whereas, in KBr or HBr solutions, the swellings are relatively slow. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 1006–1013, 2000 相似文献
17.
M. G. Koroleva O. V. Dyablo A. F. Pozharskii E. V. Sennikova Z. A. Starikova 《Russian Journal of Organic Chemistry》2005,41(7):997-1004
The corresponding N-nitroso derivatives were synthesized by the action of nitrous acid on N,N,N′-trimethylnaphthalene-1,8-diamine, N,N,N′-trimethyl-5-nitronaphthalene-1,8-diamine, and N,N,N′-trimethylacenaphthene-5,6-diamine, and molecular structure of the products was studied.__________Translated from Zhurnal Organicheskoi Khimii, Vol. 41, No. 7, 2005, pp. 1020–1027.Original Russian Text Copyright © 2005 by Koroleva, Dyablo, Pozharskii, Sennikova, Starikova. 相似文献
18.
Aliphatic and aromatic 1,3‐dithiane are oxidized to the corresponding carbonyl compounds in good yields under mild conditions by N,N′‐diiodo‐N,N′‐1,2‐ethanediyl‐bis(p‐toluenesulphonamide) [NIBTS] and silver nitrate. 相似文献
19.
Jürg K. Schneider Peter Hofstetter Ern Pretsch Daniel Ammann Wilhelm Simon 《Helvetica chimica acta》1980,63(1):217-224
N,N,N′,N′-Tetrabutyl-3,6-dioxaoctane-dithioamide, an Ionophore with Selectivity for Cd2+ The dioxa-dithioamide 3 behaves as a highly selective ionophore for Cd2+ in solvent polymeric membranes. It induces cation-permselectivity in these membranes with a transference number of 1 for Cd(NO3)2- and of 2 for CdCl2-solutions. In the presence of a proton carrier, 3 may be used to selectively pump Cd2+ through membranes by coupling with a pH gradient. 相似文献
20.
Liang Shen 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(12):m588-m590
In the crystal structure of the title compound, [Cu(NCS)2(C12H30N6O2)], the Cu atom lies on an inversion centre and has an elongated octahedral coordination, with Cu—N distances of 2.004 (2) and 2.015 (2) Å, and a Cu—S distance of 2.9696 (10) Å. The 2,2′‐ethanol chains are axially oriented. The molecules are linked to form a three‐dimensional network via O—H?N, N—H?O and N—H?S hydrogen bonds. 相似文献