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1.
Walter M. F. Fabian Gert Kollenz Yunus Akcamur Tevfik Riza Kök Makbule Teczan Mehmet Akkurt Wolfgang Hiller 《Monatshefte für Chemie / Chemical Monthly》1992,123(3):265-275
Summary 4-Benzoyl-5-phenylfuran-2,3-dione (1) and the urethanes2 combine under loss of carbon monoxide yielding the open chain dibenzoylacetic acid derivatives3 and4. 3a, b only can be cyclized to the oxazinone5. The keto-enole tautomerism3 4 is further investigated with aid of semiempirical quantum chemical calculations, based upon the molecular geometry of3a, deduced from an X-ray study.
Frau Univ. Prof. Dr. Helga Wittmann mit den besten Wünschen zum 70. Geburtstag gewidmet. 相似文献
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Phthalocyanines with four naphthyl-malonic ester groups on the periphery were synthesized by cyclotetramerization of 4-(1,1-dicarbethoxy-2-(1-naphthyl)-ethyl)-phthalonitrile.
The new compounds were characterized by spectroscopic methods. The electronic spectra exhibit intense π–π* transitions from
the naphthyl moiety together with the characteristic Q and B bands of the phthalocyanine core. The electrochemical properties
of the 2,9,17,23-tetra-(1,1-(dicarbethoxy)-2-(1-naphthyl)-ethyl) phthalocyaninato copper(II) complex were studied by cyclic
voltammetry. 相似文献
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The synthesis, characterization and voltammetric and spectroelectrochemical properties of newly synthesized metal-free and
metallo phthalocyanines (M = Co, Cu, Zn) containing four dialkylaminophenoxy or trialkylammoniumphenoxy substituents on peripheral
positions have been presented in this work. The new compounds have been characterized by using elemental analysis, UV–Vis,
FT-IR, 1H NMR and MS spectroscopic data. Phthalocyanines with trialkylammoniumphenoxy substituents are soluble in aqueous solution
over a wide pH range, and these compounds are present as aggregated species in solution as confirmed by the blue shift of
Q-bands in their electronic spectra. The electrochemical behavior of the phthalocyanines was investigated by cyclic voltammetry
and differential pulse voltammetry on a platinum-working electrode in DCM and DMSO. The voltammetric and spectroelectrochemical
measurements of the complexes show that while cobalt phthalocyanine gives both ligand- and metal-based redox processes, metal-free,
zinc and copper phthalocyanine complexes give only ligand-based processes in harmony with common phthalocyanine complexes. 相似文献
6.
Gürsoy Süleyman Koçak Makbule Cihan Ali Gül Ahmet Bekaroğlu Özer 《Transition Metal Chemistry》2000,25(4):474-477
A new soluble vic-dioxime ligand namely 1,4-bis(2′-hydroxyethyl)-2,3-bis(hydroxyimino)-5,6-diphenylpiperazine, (LH2) containing optically active centers has been prepared as a mixture of isomers from (CNO)2 and N,N-bis(2-hydroxyethyl)stilbendiamine (1) which has been made by the reduction of the condensation of the product of benzaldehyde and 2-aminoethanol in the presence
of aluminum amalgam. N,N-coordinated planar metal complexes of this ligand have been synthesized with NiII, CuII, CoII, PdII and UVIO2. Oxidation of (LH)2Co in the presence of a base, such as pyridine, leads to an octahedral complex (LH)2CopyCl containing pyridine and chloride as axial ligands in addition to vic-dioxime ligands. The structures of the ligand and its complexes are proposed on the basis of elemental analysis, 1H-n.m.r., mass, i.r. and u.v.–vis. spectral data.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
7.
Süleyman Gürsoy Ali Cihan Makbule B. Koçak Oüzer Bekaroğlu 《Monatshefte für Chemie / Chemical Monthly》2001,132(7):813-819
Summary. A novel phthalodinitrile derivative carrying dimethylaminoethylsulfanyl groups at positions 4 and 5 was synthesized from
2-dimethylaminoethanethiol hydrochloride and 1,2-dichloro-4,5-dicyanobenzene. Its cyclotetramerization in the presence of
2-dimethylamino-ethanol or metal salts (CoCl2, Zn(OAc)2) gave metal-free or metal-containing phthalocyanines (M = Co or Zn). These phthalocyanines were converted into water soluble quaternized products by reaction with methyl iodide.
The new compounds were characterized by elemental analysis, IR, NMR, and electronic spectra. 相似文献
8.
Emre GÜZEL Fatih S
NMEZ Sultan ERKAN Kübra IKRIKI Adem ERGÜN Nahit GENER Oktay ARSLAN Makbule B KOAK 《Turkish Journal of Chemistry》2020,44(6):1565
The investigation of carbonic anhydrase and paraoxonase enzyme inhibition properties of water-soluble zinc and gallium phthalocyanine complexes ( 1 and 2 ) are reported for the first time. The binding of p-sulfonylphenoxy moieties to the phthalocyanine structure favors excellent solubilities in water, as well as providing an inhibition effect on carbonic anhydrase (CA) I and II isoenzymes and paraoxonase (PON1) enzyme. According to biological activity results, both complexes inhibited hCA I, hCA II, and PON1. Whereas 1 and 2 showed moderate hCA I and hCA II (off-target cytosolic isoforms) inhibitory activity (Ki values of 26.09 µM and 43.11 µM for hCA I and 30.95 µM and 33.19 µM for hCA II, respectively), they exhibited strong PON1 (associated with high-density lipoprotein [HDL]) inhibitory activity (Ki values of 0.37 µM and 0.27 µM, respectively). The inhibition kinetics were analyzed by Lineweaver–Burk double reciprocal plots. It revealed that 1 and 2 were noncompetitive inhibitors against PON1, hCA I, and hCA II. These complexes can be more advantageous than other synthetic CA and PON inhibitors due to their water solubility. Docking studies were carried out to examine the interactions between hCA I, hCA II, and PON1 inhibitors and metal complexes at a molecular level and to predict binding energies. 相似文献
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Elif Ece İlter Nuran Asmafiliz Zeynel Kılıç Leyla Açık Makbule Yavuz E. Burcu Bali Ali Osman Solak Fevziye Büyükkaya Hakan Dal Tuncer Hökelek 《Polyhedron》2010
The reactions of hexachlorocyclotriphosphazatriene, N3P3Cl6, with N-alkyl-N-ferrocenylmethylethylene diamines, FcCH2NH(CH2)2NHR1 [R1 = Me (1) and Et (2)], and sodium [3-(N-ferrocenylmethylamino)-1-propanoxide] (3) produce spirocyclic monoferrocenyl tetrachlorophosphazenes (1a–3a). The tetrapyrrolidinophosphazenes (1b–3b) are prepared from the reactions of corresponding phosphazenes (1a–3a) with excess pyrrolidine. The reaction of 1a with excess morpholine affords geminal-morpholino phosphazene (1c), whilst the reactions of 2a and 3a give diethylaminotrimorpholino (2c) and fully substituted morpholino products (3c), respectively. The structural investigations of the compounds are examined by Fourier transform IR, MS, 1H, 13C, 31P NMR, DEPT, HETCOR, and HMBC techniques. The crystal structures of 3b and 3c are determined using X-ray crystallography. Cyclic voltammetric and chronoamperometric data show that compounds 1a–3a, 1b–3b, and 1c–3c exhibit electrochemically reversible one-electron oxidation of Fc redox centers which are hardly affected by the substituents on the phosphazene ring. The compounds 1b, 2b, 3b, and 3c are screened for antibacterial activities against Gram-positive and Gram-negative bacteria and for antifungal activities against yeast strains. In addition, the antituberculosis activities (in vitro) of these compounds are evaluated against INH-susceptible reference strain M. tuberculosis H37Rv, and six multi-drug resistant clinical M. tuberculosis isolates. Compound 2b is found to be the most active against the susceptible the reference strain. In addition, 1b, 2b, and 3c are active against all the multidrug-resistant clinical isolates at the highest concentrations. Gel electrophoresis data indicate that the compounds promote the formation of strand breaks in plasmid DNA. Almost all the concentrations lost of supercoiled DNA suggests that the compound 3b is very efficient plasmid-modifier. The compounds inhibit BamHI cleavage of pUC18 DNA while restricting HindIII. 相似文献