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971.
铜(II)-5-取代邻菲啰啉-二氧四胺大环三元体系的稳定性研究 总被引:1,自引:0,他引:1
The stability of copper (Ⅱ)-13-(2'-Hydroxy-3',5'-substituted benzyl)-1,4,8,11-tetraazacyclotetradecane-12, 14-dione(RTADO-14) binary complex compounds and of copper (Ⅱ)-5-substituted-1,10-phenanthrolines(R'TADO)-RTADO-14 ternary complex compounds was studied by means of pH titration method at 25.0±0.1 ℃ and I=0.1mol?dm-3KNO3. The formation constants of binary and ternary complexes were obtained. The structures of the binary and ternary complxes and the effects fo substituents on macrocyclic ligands and on R'Phen were also discussed. 相似文献
972.
973.
The coordination compounds of acctylacetonate-5,10,15,20-tctrasubstituted phcnyl-porphyrin with Yttrium, Y(o-Cl)Tppacac, Y(m- Cl)Tppacac, Y(p-Cl)Tppacac, Y(o-CH3O) Tppacac, and Y(p-CH3O)Tppacac (H2Tpp: tetraphcnylporphyrin, Hacac: acetylacctonc), were prepared and characterised on the basis of elemental analysis, infrared spectra, UV-visiblc spectra and thermal analysis. 相似文献
974.
975.
0 IntroductionIn recent years, silver carboxylates have attractedmany interests, mostly because they are promisingcandidates in the growth of metal thin films via metal-organic chemical vapor deposition (MOCVD) tech-niques. These sliver compounds show low light sensi-tivity and relatively high thermal stability. Several ex-amples of bisphosphine ligands coordinated silver car-boxlylates have been reported[1 ̄4].Monophosphine coordinated silver complexes areexpected to have better volatility,… 相似文献
976.
Cobalt(Ⅱ) can form complexes with Hdbm in different environments. Hdbm reacted with cobalt nitrate to give complex 1 [Co(dbm)2·2H2O]. When complex 1 reacted with pyridine, α-stilbazole or 4,4′-bipyridine respectively, complex 2 [Co(DBM)2Py2] (Py=pyridine), 3 [Co(DBM)2Sbz2] (Sbz=α-stilbazole) or 4 [Co(DBM)2BPy]n was obtained in turn through metathetical reaction. The coordination modes are octahedral polyhedrons. In the crystal structures, the two dbms take the plane position and two other donor molecules take the axial position. CCDC: 196070 for complex 2; 186859 for complex 3. 相似文献
977.
采用非晶态多核配合的方法合成了La1-xCuxMnO3(x=0、0.05、0.1、0.2、0.3、0.4、0.5)系列催化剂, 并用X射线衍射(XRD)、透射电镜(TEM)、比表面测定仪(BET)等手段对催化剂的微观结构进行了表征. 研究了Cu掺杂对钙钛矿结构及其对CO催化氧化发光性能及催化氧化CO、CH4性能的影响规律. 结果表明, 当x≤0.1 时, Cu掺杂仍可形成单相的钙钛矿结构; 当x>0.1时, 过量掺杂的Cu以CuO杂相存在. Cu掺杂可改善La1-xCuxMnO3催化剂对CO和CH4的催化氧化活性. 经700 ℃焙烧3 h制备的La0.9Cu0.1MnO3催化剂具有最高CO催化氧化活性(T100%=170 ℃), 该结果与CO催化氧化发光结果一致.而La0.95Cu0.05MnO3催化剂对CH4的催化氧化活性最高(T95%=705 ℃). 相似文献
978.
A determination method has been optimized and validated for the simultaneous analysis of tetracycline (TC), oxytetracycline (OTC), chlortetracycline (CTC) and doxycycline (DC) in honey. Tetracyclines (TCs) were removed from honey samples by chelation with metal ions bound to small Chelating Sepharose Fast Flow columns and eluted with Na2EDTA-Mcllvaine pH 4.0 buffers. Extracts were further cleaned up by Oasis HLB solid-phase extraction (SPE), while other solid-phase extraction cartridges were compared. Chromatographic separation was achieved using a polar end-capped C 18 column with an isocratic mobile phase consisting of oxalic acid, acetonitrile and methanol. LC with ultraviolet absorbance at 355 nm resulted in the quantitation of all four tetracycline residues from honey samples fortified at 15, 50, and 100 ng/g, with liner ranges for tetracyclines of 0.05 to 2 μg/mL. Mean recoveries for tetracyclines were greater than 50% with R.S.D. values less than 10% (n= 18). Detection limits of 5, 5, 10, 10 ng/g for oxytetracycline, tetracycline, chlortetracycline and doxycycline, respectively and quantitation limits of 15 ng/g for all the four tetracyclines were determined. Direct confirmation of the four residues in honey (2-50 ng/g) was realized by liquid chromatography-tandem mass spectrometry (LC/MS/MS). The linear ranges of tetracyclines determined by LC/MS/MS were between 5 to 300 ng/mL, with the linear correlation coefficient r〉 0.995. The limits of detection of 1 to 2 ng/g were obtained for the analysis of the TCs in honey. 相似文献
979.
Crystal structure of the title compound, Cu(phen)(H2O)2·ClO4(phen=1,10-phenanthroline), was deter-mined by X-ray crystallography. It crystallizes in the monoclinic system, space group C2/c with lattice parameters a=1.49071(4)nm, b=1.38594(4)nm, c=0.70292(1)nm, β=108.509(1)° and Z=4; The Cu(Ⅰ) ion is chelated by a phen ligand and two aqua ligands in cis arrangement and assumes a C2 symmetric square-planar geometry with the CuN2O2 core. Eight Cu(phen)(H2O)2·ClO4 molecules are interconnected by strong hydrogen bonds between coordinated water molecules and uncoordinated perchlorate anions to form a molecular scale cavities along c axis. The bond distances of Cu-N and Cu-O are 0.2003(4)nm and 0.1973(3)nm, respectively. CCDC: 197600. 相似文献
980.
DNA works as hereditary material and plays vital role in life science. The study of the binding of small molecules complex to DNA has been the focus of intense investigation, owning to their stereo and sequence specific interaction with the double helix1-… 相似文献