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1.
The preparation of 6,6′-dibromo-2,2′-bipyridine and 6-bromo-2,2′-bipyridine are described. The dibromo compound was prepared by way of an improved cuprate synthesis resulting in a 72% yield. The monobromo species was prepared from the dibromo compound by way of metal-halogen exchange in 88% yield. 相似文献
2.
XinHuaXU RuiLiangLU BingZHOU JianPingLI YinQuanDENG 《中国化学快报》2004,15(2):145-147
The title compound 5 was synthesized in 45% yield by the reaction of compound 3 with α,α′-bis (bromomethyl)-2, 2′-bipyridine in CH3CN at 70℃ for 24 h. 相似文献
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4.
The inorganic-organic coordination polymer infin; 2[Cu2I2(μ-4-4′-bipyridine)] was prepared by the reaction of Cu(I)I and 4,4′-bipyridine in acetonitrile. Its structure consists of staircase-like CuX double chains which are connected to sheets by the 4,4′-bipyridine ligands. The thermal decomposition of the corresponding 1:1 copper(I) halide-4,4′-bipyridine compounds infin; 2[CuX(μ-4-4′-bipyridine)] (X = Cl, Br, I) was investigated using simultaneous difference thermal analysis and thermogravimetry (DTA-TG), thermomicroscopy, and temperature resolved X-ray powder diffraction in air or argon. Upon heating infin; 2[CuX(μ-4-4′-bipyridine)], several changes in sample mass are observed which correspond to a stepwise loss of the organic ligands. Temperature-resolved X-ray powder diffraction proves that infin; 2[CuX(μ-4-4′-bipyridine)] transforms to infin; 2[Cu2 X 2(μ-4-4′-bipyridine)] during the decomposition; the latter looses the remaining ligands when heated further, forming the corresponding copper(I)halides. When the experiments were performed under an argon atmosphere, the 2:1 coordination polymers were obtained as phase-pure compounds. 相似文献
5.
ZHANG Jun-feng GAN Xin OU Xue-mei FU Wen-fu 《高等学校化学研究》2007,23(6):679-682
Two novel cyclotriphosphazene derivatives containing 6- (4-hydroxyphenyl)-2,2′-bipyridine (hopbp) side groups, N3 P3 (dobp) 2 (hopbp) 2 ( 1 ) and N3 P3 (dobp) (hopbp) 4 (2) ( dobp = 2,2′-dioxybiphenyl), were synthesized and characterized. These compounds display strong fluorescent emission both in solution and in solid state. Their absorption and emission spectra are sensitive to proton: the addition of HBF4 to the methanol and dichloromethane solution(9: 1, volume ratio) of compound 1 led to a red-shift from 350 to 460 nm for the emission spectrum, and the process was also characterized by isosbestic points of absorption spectra at 267, 287 and 313 nm. 相似文献
6.
《Solid State Sciences》2012,14(8):1055-1059
Homochiral framework materials are of current interest due to their potential applications in asymmetric catalysis and enantioselective separation. Four new Cd(II) camphorates (1–4) with 2,2′-bipyridine ligand (= 2,2′-bipy) are successfully synthesized and show distinct structural features. Such rich Cd-cam-2,2′-bipy system is composed of four compounds, [Cd(d-cam)(2,2′-bipy)(DMF)]n (1), [Cd(d-cam)(2,2′-bipy)(H2O)]n (2), [Cd2(d-cam)2(2,2′-bipy)2]n (3) and [Cd2Cu2(d-cam)4(2,2′-bipy)2]n·4nH2O (4), which are obtained under different conditions. Both compounds 1 and 2 show infinite homochiral Cd-camphorate chain, while compounds 3 and 4 exhibit homochiral layered structures based on different dinuclear units. The results demonstrate the rich coordination chemistry of the enantiopure d-camphorate ligand and the structural diversity of metal-camphorate compounds. 相似文献
7.
A convenient and high yield preparation of 4, 4′-dicarboxy-2, 2′-bipyridine from the oxidation 4, 4′-dimethyl-2, 2′-bipyridine with potassium dichromate in sulfuric acid is reported. 相似文献
8.
Values of the condensed phase standard (p = 0.1 MPa) molar enthalpy of formation for 2′- and 4′-methylacetophenones were derived from the standard molar energies of combustion, in oxygen, at T = 298.15 K, measured by static bomb combustion calorimetry. The values of the standard molar enthalpy of vaporization, at T = 298.15 K, were measured by Calvet microcalorimetry. Combining these two values, the following enthalpies of formation in the gas phase, at T = 298.15 K, were then derived: 2′-methylacetophenone, –(115.7 ± 2.4) kJ · mol−1, and 4′-methylacetophenone, –(122.6 ± 2.4) kJ · mol−1. Substituent effects are discussed in terms of stability and compared with other similar compounds. The value of the standard molar enthalpy of formation for 3′-methylacetophenone was estimated from isomerization schemes. 相似文献
9.
《Tetrahedron letters》1987,28(23):2623-2626
2′-5′,3′-5′ Linked triadenylates have been synthesized by direct bisadenylylation of adenosine 2′ and 3′ hydroxyls with an adenosine 5′-phosphorochloridite followed by oxidation. 相似文献
10.
The title compounds, 4'-0-geranylisoliquiritigenin and 4'-0-geranylnaringenin isolated from Millettia ferruginea and Borania coerulescens respectively, were first synthesized starting from geranyl bromide, 4-hydroxybenzaldehyde and O-hydroxy acetophenones by the condensation reaction and demethoxymethylation as key steps. 相似文献
11.
《Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy》1991,47(12):1727-1733
Molecular charge-transfer complexes of 2,2′-bipyridine with iodine and tetracyanoethylene have been investigated. The formation constants of these complexes were determined at different temperatures and the thermodynamic functions, ΔHf and ΔSf were calculated. The spectra and stability of the complexes were discussed and interpreted. 相似文献
12.
Noha Said Bedowr Rosiyah Binti Yahya Nesrain Farhan 《Journal of Saudi Chemical Society》2018,22(3):255-260
This paper presents synthesis, structural characterization and spintronic applications of copper (II) tetradecanoate derived magnetic complexes. The complexes were prepared by a chemical reaction between [Cu2(CH3(CH2)12COO)4](EtOH)2 and 2,2′-bipyridine-4,4′-bipyridine ligands respectively. The complexes were further reacted between the product of the first reaction and 4,4′-bipyridine-2,2′-bipyridine respectively. The structural characterization techniques included elemental analysis, Fourier transformed infrared spectroscopy (FTIR), Ultra-violet–Visible (UV–Vis) spectroscopy, polarized optical microscopy, magnetic moment and thermogravimetric analysis. The structural and characterization results suggested that the synthesized complexes were binuclear and mononuclear covalent complexes of copper(II) with structural formulas [Cu2(η2-(OOCR)4](4,4′-bpy)2H2O] and [Cu(η1-(OOCR)2(2,2′-bpy) (4,4′-bpy)] respectively. 相似文献
13.
Slepukhin P. A. Krinochkin A. P. Starnovskaya E. S. Shtaitz Ya. K. Savchuk M. I. Kopchuk D. S. Egorov I. N. Santra S. Zyryanov G. V. Chupakhin O. N. 《Russian Chemical Bulletin》2022,71(7):1533-1543
The structures of six 2,2′-bipyridine derivatives containing aromatic amine moieties, namely N-aryl-4-aryl-1-(pyridin-2-yl)-6,7-dihydro-5H-cyclopenta[c]pyridine-3-amines, were studied by single-crystal X-ray diffraction. The molecular structures and the effect of the substituents of these compounds on the crystal packing are discussed.
相似文献14.
15.
I. Victor Ekhato 《合成通讯》2013,43(16):2341-2349
(4′R)- and (4′S)-Spiro(oxirane-2,4′-5α-cholestan-3′β-ol) (1) and (2) were made from (4′R)- and (4′S)-spiro(oxirane-2,4′-5α-cholestan-3-one) (8) and (9). Alkaline hydrogen peroxide oxidation of 4-methylene-5α-cholestan-3-one (7) gave compounds (8) and (9) as a readily separable (1:1) mixture. Reduction of (9) to (2) provided access to a compound which could not be made by other methods. 相似文献
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17.
Peng Song Shi-guo Sun Pan-wang Zhou Jian-yong Liu Yong-qian Xu Xiao-jun Peng 《化学物理学报(中文版)》2010,23(5):558-564
Spectral and photophysical investigations of 4′-(p-aminophenyl)-2,2′:6′,2′′-terpyridine (APT) have been performed in various solvents with different polarity and hydrogen-bonding ability.The emission spectra of APT are found to exhibit dual fluorescence in polar solvents, which attributes to the local excited and intramolecular charge transfer states, respectively. The two-state model is proven out for APT in polar solvent by the time-correlated single photon counting emission decay measurement. Interestingly, the linear relationships of different emission maxima and solvent polarity parameter are found for APT in protic and aprotic solvents, because of the hydrogen bond formation between APT and alcohols at the amino nitrogen N25. Furthermore, the effects of the complexation of the metal ion with tpy group of APT and the hydrogen bond formation between APT with methanol at the terpyridinenitrogen N4—N8—N14 are also presented. The appearance of new long-wave absorption and fluorescence bands indicates that a new ground state of the complexes is formed. 相似文献
18.
Aleksandriiskii V. V. Novikov I. V. Monakhov L. O. Burmistrov V. A. 《Russian Journal of General Chemistry》2021,91(3):559-563
Russian Journal of General Chemistry - The formation of a chiral nematic mesophase by doping a liquid crystalline mixture of 4-alkyloxy-4′-cyanobiphenyls with chiral... 相似文献
19.
《Vibrational Spectroscopy》2004,34(2):269-272
The adsorption structure and mechanism of 4,4′-bipyridine (BiPy) on gold nanoparticle surfaces has been investigated by means of surface-enhanced Raman scattering (SERS). The aromatic ring of BiPy appeared to assume a perpendicular orientation with respect to the gold surface from the presence of the ν(CH) band at ∼3060 cm−1. The SERS intensities of several vibrational modes of BiPy on Au were found to vary as the bulk concentration. The SERS intensities for BiPy on Au could be ascribed to both the electromagnetic (EM) and charge transfer (CT) enhancement mechanism. 相似文献
20.
《合成通讯》2013,43(17):3071-3076
Abstract The treatment of 4-(2′-hydroxyaryl)-2-(N,N-dialkylamino)-1,3-dithiolium perchlorates (1a–g) with sodium sulfide nonahydrate in ethanol at room temperature affords the corresponding 1,3-dithiole-2-thiones (2a–g). When these reactions are conducted in boiling ethanol, 2′-hydroxyacetophenones (3a–g) have been obtained in good to excellent yield. A tentative mechanism for the formation of 3a–g shows that this reaction is regioselective, this being established by the presence of hydroxyl group in 2′-position. That has been confirmed in a control experiment, 4-phenyl-2-(piperidin-1-yl)-1,3-dithiolium perchlorate affording a mixture of condensation products of acetophenone and phenylacetaldehyde, under similar reaction conditions. 相似文献