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1.
Salts ofN-(β-hydroxyalkyl)-N′-hydroxydiazeneN-oxides, RCH(OH)CH2N(O)=NO− M+ (R=Me, Pri, or But; and M=Li, Na, K, Ag, NH4, or Me4N), were prepared. Their alkylation with alkyl halides R′X (X=Cl, Br, or I) and dimethyl sulfate was studied. Generally, alkylation
afforded mixtures ofN-(β-hydroxyalkyl)-N′-alkoxydiazeneN-oxides RCH(OH)CH2N(O)=NOR′ andO-alkyl-N-(β-hydroxyalkyl)-N-nitrosohydroxylamines RCH(OH)CH2N(NO)OR′.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1996–2001, October, 1998. 相似文献
2.
Kukharev B. F. Stankevich V. K. Klimenko G. R. Lobanova N. A. Kovalyuk E. N. Negoda A. Yu. Stankevich V. V. Bragin E. V. 《Russian Journal of Applied Chemistry》2010,83(9):1666-1667
N-(2-Vinyloxyethyl)-N′-cyclohexylidene-1,2-ethylenediamine and N,N′,N″-tris-[2-(2-vinyloxyethyl)-aminoethyl]hexahydro-1,3,5-triazine were synthesized by reactions of N-(2-vinyloxyethyl)-1,2-ethylenediamine with cyclohexanone and formaldehyde with yields of 91 and 90%, respectively. The IR
and 1H and 13C NMR spectral data and the results of studying their anticorrosion properties are given. 相似文献
3.
Zhiping Wu Yu Chen Xu Feng Bing Xia Ming Wang Yunfa Dong 《Chemistry of Natural Compounds》2010,46(2):187-191
From the the bulbs of Zephyranthes candida (Amaryllidaceae), another two novel ceramides have been isolated and identified. The structures of the two novel compounds
were established as (2S,3S,4R,21E,2′R)2-[N-(2′-hydroxynonadecanoyl)-N-(1′′,2′′-dihydroxyethyl)amino]-21-hexacosene-1,3,4-triol, named zephyranamide C (1), and 1,3,4,5,6-pentahydroxy-2-(2′-hydroxyhexacosanoyl-amino)-18-(E)-tetracosene, named zephyranamide D (2). Their structures and stereochemistries were elucidated by spectral techniques including 1H NMR, 13C NMR, as well as HSQC, HMBC, DEPT, and COSY. 相似文献
4.
O. G. Khudina E. V. Shchegol’kov Ya. V. Burgart V. I. Saloutin D. V. Bukhvalov D. V. Starichenko Yu. N. Shvachko A. V. Korolev V. V. Ustinov G. G. Aleksandrov I. L. Eremenko O. N. Kazheva G. V. Shilov O. A. D’yachenko O. N. Chupakhin 《Russian Chemical Bulletin》2007,56(1):108-114
The crystal structures of the chelates NiIIL (L2− are the N,N′-(o-phenylene)-bis[4-(4-methylphenyl)hydrazono-3-oxo-1,1,2,2-tetrafluorononane-5-iminate], N,N′-ethylene-bis[3-(4-methylphenyl)hydrazono-4-oxo-5,5,6,6,7,7,8,8-octafluorooctane-2-iminate], or N,N′-ethylene-bis(4-hydroxy-5,5,6,6,7,7,8,8-octafluoro-3-octene-2-iminate) anions) were studied by X-ray diffraction. Magnetic
measurements and ESR spectroscopic studies revealed the appearance of paramagnetism due to a tetrahedral distortion of the
coordination unit and also the unusual behavior of the effective magnetic moment at low temperatures.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 103–109, January, 2007. 相似文献
5.
Depending on the reactant ratio, dithiooxamide (ethanedithioamide) reacted as N-nucleophile or N,N′-binucleophile with highly
electrophilic aldimines, N-(2,2,2-trichloroethylidene)- and N-(2,2-dichloro-2-phenylethylidene)arenesulfonamides, to give the corresponding mono- or bis-adducts, N-[2-polychloro-1-(arylsulfonylamino) ethyl]ethanedithioamides or N,N′-bis[2-polychloro-1-(arylsulfonylamino)ethyl]ethanedithioamides, in good yield. 相似文献
6.
Muhammad Mufakkar Anvarhusein A. Isab Tobias Rüffer Heinrich Lang Saeed Ahmad Najma Arshad Abdul Waheed 《Transition Metal Chemistry》2011,36(5):505-512
Copper(I) complexes of thioureas having the general formulae [CuLnBr] and [CuLn]Br [where, n = 1 − 4 and L = thiourea (Tu), N-methylthiourea (Metu), N-ethylthiourea (Ettu), N,N′-dipropylthiourea (Dprtu), N,N′-dibutylthiourea (Dbtu) or N,N′-diphenylthiourea (Dphtu)] were prepared and characterized by elemental analysis, IR, and NMR (1H and 13C) spectroscopy. The crystal structure of one of them, [Cu(Metu)4]Br (1), was determined by X-ray crystallography. The X-ray structure of 1 describes a tetrahedral geometry around copper(I) with all Metu ligands binding through sulfur atoms. An upfield shift in
the 13C NMR and downfield shift in the 1H NMR spectra are consistent with the thione coordination to copper(I). Antimicrobial activities of the complexes were evaluated
by the minimum inhibitory concentration method. The results showed that only [Cu(Ettu)3Br] was effective in inhibiting the growth of all the tested organisms (gram-positive, gram-negative bacteria, and Candida sp.), while the other complexes were not effective against all the organisms. 相似文献
7.
Shuji Fujisawa Yusuke Okita Tsuguyuki Saito Eiji Togawa Akira Isogai 《Cellulose (London, England)》2011,18(5):1191-1199
A method for conversion of carboxyl groups present on the surface of TEMPO-oxidized cellulose nanofibrils to N-acylureas using carbodiimide was developed. A TEMPO-oxidized cellulose nanofibril with free carboxyl groups (TOCN–COOH) dispersed
in N,N-dimethylformamide (DMF) is prepared from a bleached kraft pulp, and then the TOCN–COOH is reacted with either N,N′-diisopropylcarbodiimide (DIC) or N,N′-dicyclohexylcarbodiimide (DCC) under apparently homogeneous conditions. FT-IR and solid-state 13C NMR analyses showed that the reaction products contained N-acylurea groups, and yields were >80%. Conversion ratios of carboxyl groups to N-acylureas are approximately 80 and 60%, when DIC and DCC, respectively, of 5 mol per mole of carboxyl groups are used as
the reagents. X-ray diffraction analysis demonstrated that neither crystallinity nor crystal width of the original wood cellulose
I structure was changed by the N-acylurea formation. The isolated and never-dried TOCN-N-acylureas are nano-dispersed in DMF but not in i-PrOH or dioxane. Pellets of the TOCN-N-acylureas had water-contact angles of >70°. 相似文献
8.
I. E. Tolpygin 《Russian Journal of Organic Chemistry》2012,48(1):104-108
A number of 2-(anthracen-9-yl)-substituted imidazolidines and hexahydropyrimidines were synthesized by reaction of N,N′-bis[aryl(hetaryl)methyl]ethylene-1,2-diamines and N,N′-bis[aryl(hetaryl)methyl]-propane-1,3-diamines with anthracene-9-carbaldehyde. The obtained compounds showed chemosensor
activity toward Cd2+, Cu2+, and Hg2+ ions. 相似文献
9.
Mohamed El-Sayed Hardy Müller Gerd Rheinwald Heinrich Lang Stefan Spange 《Monatshefte für Chemie / Chemical Monthly》2003,134(3):361-370
Summary. N-(2′-Hydroxy-4′-N,N-dimethylaminobenzylidene)-4-nitroaniline [HDBN] has been used as a model for investigating intra- and intermolecular D–A (donor–acceptor) interactions in various environments
by means of UV/Vis spectroscopy. UV/Vis spectra of HDBN have been measured in various solvents, ethanolic solutions of different pH, adsorbed on silica, and in the solid state. A bathochromic shift of νmax is observed with increasing the dipolarity/polarizability and HBD (hydrogen bond donor) capacity of the solvent, which is
described by means of a multiple LSE (linear solvation energy) relationship in terms of the empirical Kamlet-Taft solvent polarity parameters. The adsorption of HDBN on Aerosil? 300-silica particles in non-HBA (hydrogen bond acceptor) solvents is explained in the same sense. Mobile protons and sol–gel
entrapping cause a hypsochromic shift due to protonation of the lone electron pair of the 4′-N,N-dimethylamino group. Hydroxide ions attack the 2′-hydroxy group which causes a bathochromic shift. A strong intramolecular
hydrogen bond between the 2′-hydroxyl hydrogen and the imine nitrogen atom is present in the solid-state structure causing
an unprecedented bathochromic shift.
Corresponding author. E-mail: stefan.spange@chemie.tu-chemnitz.de
Received July 8, 2002; accepted (revised) September 30, 2002 相似文献
10.
Three novel tripodal ligands, N,N′,N′′-tri-(3′-phenylpropionic acid-2′-yl-)-1,3,5-triaminomethylbenzene (Ll), N,N′,N′′-tri-(4′-methylvaleric acid-2′-y1-)-1,3,5-triaminomethylbenzene (L2) and N,N′,N′′-tri-(3′methylvaleric acid-2′-yl-)-1,3,5-triaminomethylbenzene (L3), have been synthesized and fully characterized. The
stabilizing ability of complexes of the three ligands with transition metal ions Cu(II), Ni(II), Zn(II) and Co(II) and rare
earth metal ions La(III), Nd(III), Sm(III), Eu(III) and Gd(III) has been investigated by the pontentiometric method in water
and in aqueous KNO3 (0.1 mol dm−3) at 25.0±0.1 °C, respectively. The results show that there is a great deal of difference between two series of complexes’
stabilities. An explanation of the difference has been given. 相似文献
11.
Hasan Marai Ewa Kita Emilia Kiersikowska Sylwia Kuchta Anna Bajek Tomasz Drewa 《Transition Metal Chemistry》2012,37(4):337-344
Three chromium(III) complexes with asparagine (Asn) and histidine (His) of the [Cr(ox)2(Aa)]2− type, where Aa = N,O–Asn, N,O–His or N,N′–His, were obtained and characterized in solution. The complexes with N,O–Aa undergo acid-catalysed aquation to give a free amino acid and cis-[Cr(ox)2(H2O)2]−, whereas the complex with N,N′–His undergoes parallel reaction paths: (1) isomerization to the N,O–His complex and (2) liberation of an oxalate ligand. Kinetics of the N,O–Aa complexes in HClO4 media were studied spectrophotometrically under pseudo-first-order conditions. The absorbance changes were attributed to
the chelate ring opening at the Cr–N bond. The linear dependence of rate constants on [H+] was established, and a mechanism for the chelate ring cleavage was postulated. The existence of a metastable intermediate
with O-monodentate Aa ligand was proved experimentally. Effect of [Cr(ox)2(Aa)]2− on 3T3 fibroblasts proliferation was studied. The tests revealed low cytotoxicity of the complexes. Complexes with Ala, His
and Cys are good candidates for biochromium sources. 相似文献
12.
L. T. Eremenko L. B. Romanova M. E. Ivanova D. A. Nesterenko V. S. Malygina A. B. Ermeev G. V. Lagodzinskaya V. P. Lodygina 《Russian Chemical Bulletin》1998,47(6):1137-1140
NewN,N′-bis- andN,N,N′, N′-tetrakis-hydroxyalkyl-substituted 1,4-cubanedicarboxamides were synthesized. Nitration of these compounds yielded the corresponding
nitrates. The reaction of 1,4-cubanedicarboxylic acid dichloride with ethylene glycol mononitrate and glycerol dinitrate gave
ester 1,4-[R1R2CHOC(O)]2C8H6, where R1=H and R2=CH2ONO2; and R1=R2=CH2ONO2, respectively. The cardiopharmacological activity of some of the synthesized compounds was determined. This allowed us to
find for the first time cubane derivatives that exhibit this kind of biological activity. The antiischemic activity of one
of these compounds,N,N′-bis(2-nitroxythyl)-1,4-cubanedicarboxdiamide, is higher than that of the well-known Nicorandil.
For Part 2, see Ref. 1.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1169–1172, June, 1998. 相似文献
13.
A. S. Gordetsov S. V. Zimina S. V. Saprykina L. B. Loginova A. V. Piskunov V. F. Ur’yash E. M. Moseeva 《Russian Journal of General Chemistry》2011,81(4):658-662
1,3,5-Tris[bis(η5-cyclopentadienyl)chlorovanadium]melamin is prepared in high yield by the reaction of N,N′-bis(trimethylsilyl)dicyandiamide with bis(η5-cyclopentadienylvanadium) dichloride in tetrahydrofuran. As side products, trimethylchlorosilane and cyclopentadiene formed.
Reaction of N,N′-bis(trimethylsilyl) dicyandiamide with benzoyl chloride results in the formation of tris(benzoyl)melamin. 相似文献
14.
Gordana P. Radi? Verica V. Glo?ovi? Goran N. Kalu?erovi? Frank W. Heinemann Sre?ko R. Trifunovi? 《Transition Metal Chemistry》2011,36(4):331-336
The reaction of K2[PdCl4] with [(S,S)-H2(Et)2eddv]Cl2 diester (O,O′-diethyl-(S,S)-ethylenediamine-N,N′-di-2-(3-methyl)butanoate) (1) resulted in [PdCl2{(S,S)-(Et)eddv-κ2
N,N′,κO}] (2) complex with one hydrolyzed ester group. The compound was characterized by spectroscopic methods and it was found that the
reaction is diastereoselective (1H and 13C NMR; one diastereoisomer of four possible). In addition, the structure of 2 was confirmed by X-ray diffraction analysis, indicating that the product is the (R,R)–N,N′-configured isomer. DFT calculations support the formation of one diastereoisomer of 2. 相似文献
15.
V. Yu. Korotaev Yu. A. Skorik A. Yu. Barkov M. I. Kodess A. Ya. Zapevalov 《Russian Chemical Bulletin》2005,54(11):2545-2549
3,3,3-Trifluoro-N′-(3-trifluoromethylphenyl)-1,2-propanediamine (5) was synthesized by the reaction of 2-diazo-1,1,1-trifluoro-3-nitropropane or 3,3,3-trifluoro-1-nitropropene with 3-aminobenzotrifluoride
followed by the reduction of the nitro group. The Michael 1,4-addition of diamine 5 to acrylic acid occurs only at the N(1) atom and affords N-mono-or N,N-dicarboxyethyl derivatives 6 and 7, depending on the reactant ratio. Protolytic equilibria 5–7 in aqueous solutions were studied by pH-potentiometry and UV spectroscopy. Only the aliphatic amino group can be protonated
in an aqueous solution, while the aromatic amino group remains unprotonated even in 12 M HCl. The stability constants of transition metal (Cu2+, Ni2+, Zn2+) complexes with ligands 5–7 were determined by pH-potentiometric titration. The stability of the complexes and selectivity of the ligands toward Cu2+ ions increase with an increase in the number of N-carboxyethyl groups.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2465–2469, November, 2005. 相似文献
16.
B. S. Fedorov N. I. Golovina V. V. Arakcheeva M. A. Fadeev G. V. Strukov V. V. Kedrov G. V. Shilov L. O. Atovmyan 《Russian Chemical Bulletin》1999,48(8):1584-1586
The reaction ofN,N′-bis(2-nitroxyethyl)pyridine-2,6-dicarboxamide with PdCl2 afforded previously unknowncis-(N-2-nitroxyethylpicolinamide-N,N′)dichloropalladium(II) andcis-[2-(2-pyridyl)-2-oxazoline-N,N′]dichloropalladium(II), which were isolated as a cocrystallizate of the molecular compounds. Its structure was established
by X-ray diffraction analysis.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1604–1606, August, 1999. 相似文献
17.
Reactions of 2-(4,5-dihydro-3-furyl)-1,3-diphenyl-1,3-diaza-2λ3-phospholidine (1) with nitrile imines are multistep processes involving cleavage of one P-N bond of the diazaphospholidine ring to form substituted
5-(2-chloroethyl)-4-(N,N′-diphenylethylenediamino)-1,4-dihydro-1,2,4λ5-diazaphosphorines 4 as final products. Analogs of phospholidine 1, namely, 4,5-dihydro-3-furylphosphonous dipiperidide and dimorpholide, react with C,N-diphenylnitrile imine with retention of both P-N bonds to give 5-(2-hydroxyethyl)-1,2,4-diazaphosphorinium chlorides.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1590–1593, July, 2005. 相似文献
18.
The equilibrium constants, K
2, have been determined for the proton-transfer reactions of 1-phenacylquinolinium ion, PHQ+, with several amines {triethylamine (TEA), N,N,N′,N′-tetramethylethylenediamine (ED), N,N,N′, N′-tetramethylpropanediamine (PD), N,N,N′,N′-tetramethylbutanediamine (BD), and 1,8-bis(dimethylamino-naphthalene (DMAN)} in acetonitrile (AN), AN-tetrahydrofuran (THF)
and AN-ethanol (EtOH) mixtures. The reaction was followed spectrophotometrically using a stopped-flow technique. The K
2 value decreased for DMAN and increased for TEA with increasing vol-% of THF in AN-THF mixtures. The changes in the K
2 value for ED, PD and BD changed in the order: ED, PD and BD from a pattern similar to TEA to a pattern similar to DMAN. The
change in the K
2 value for DMAN with increasing vol-% of THF in AN-THF mixtures was explained by the effect of polarity on the stability of
P−Q+ (the deprotonated product of PHQ+). The effect of THF on the K
2 value is consistent with that of the peak wavelength of the absorption spectrum of P−Q+. The change in the K
2 value for TEA, ED, PD and BD depended on the structures of the protonated bases, one of the products for this reaction. The
effect of EtOH on the K
2 value for DMAN was examined in ternary EtOH-THF-AN mixtures that contain different amounts of EtOH and whose relative permittivities
were adjusted to that of EtOH. The K
2 value increased with increasing vol-% of EtOH because of the stabilization of P−Q+ upon the formation of the hydrogen-bonded complex with EtOH. The absorption spectrum of P−Q+ demonstrated a blue shift as the vol-% of EtOH increased. 相似文献
19.
Hassan Keypour Reza Azadbakht Hadi Amiri Rudbari Alireza Heydarinekoo Hamidreza Khavasi 《Transition Metal Chemistry》2009,34(8):835-839
Three new potentially hexadentate N4O2 Schiff-base ligands (H2L1, H2L2 and H2L3) were prepared from the reaction of the polyamines N,N′-bis(2-aminophenyl)-1,2-ethanediamine (L1), N,N′-bis(2-aminophenyl)-1,3-propanediamine (L2) and N,N′-bis(2-aminophenyl)-1,4-butanediamine (L3), respectively with salicylaldehyde. Reaction of the Schiff bases with Ni(II) salts in the presence of N(Et)3 gave the neutral complexes [NiL4], [NiL5] and [NiL6]. Ni(II) complexes of the polyamines were also prepared. One of complexes [Ni(L1)(MeCN)2](ClO4)2·MeCN has been characterized through X-ray diffraction methods. 相似文献
20.
Two multidentate ligands: N,N′-di-(propionic acid-2′-yl-)-2,9-di-aminomethylphenanthroline (L1) and N,N′-di-(3′-methylbutyric acid-2′-yl-)-2,9-di-amino-methylphenanthroline (L2) were synthesized and fully characterized by 1H NMR and elemental analysis. The binding ability of L1 and L2 to metal ions such as M(II) (M = Cu, Zn, Co and Ni) and Ln(III) (Ln = La, Nd, Sm, Eu, and Gd) has been investigated by potentiometric
titration in aqueous solution and 0.1 mol dm−3KNO3 at 25.0 ± °C. In view of the structure of L1 and L2, mononuclear metal complexes can be formed in solution. The stability constants of binary complexes of ligands L1 and L2
with metal ions M(II) and Ln(III) have been determined respectively and further discussed. 相似文献