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861.
862.
The Cr-Cr singly-bonded dimers [{η5-RC5H4Cr(CO)3}2] (1, R=Me; 2, R=CO2Et) reacted with an equivalent of elemental selenium in THF at room temperature to give the linear Cr2Se complexes [{η5-RC5H4Cr(CO)2}2Se] (3, R=Me; 4, R=CO2Et), whereas the linear Cr2Se complex (5, R=MeCO) reacted with excess NaBH4, Ph3PCHPh or 2,4-dinitrophenylhydrazine under respective conditions to afford the linear Cr2Se derivatives [{η5-RC5H4Cr(CO)2}2Se] (6, R=MeCH(OH); 7, R=PhCHCMe; 8, R=2,4-(NO2)2C6H3NHNCMe). Similarly, while the butterfly Cr2Se2 complexes [{η5-RC5H4Cr(CO)2}2Se2] (9, R=Me; 10, R=CO2Et) could be produced either by reaction of dimers 1 and 2 with an excess amount of elemental selenium, or by reaction of the linear complexes 3 and 4 with an equivalent of elemental selenium, the butterfly Cr2Se2 derivatives [{η5-RC5H4Cr(CO)2}2Se2] (12, R=MeCH(OH); 13, R=PhCHCMe; 14, R=2,4-(NO2)2C6H3NHNCMe) were yielded by reaction of the butterfly Cr2Se2 complex (11, R=MeCO) with an excess quantity of NaBH4, Ph3PCHPh and 2,4-dinitrophenylhyazine. Both the linear complexes 3, 4, 6-8 and the butterfly complexes 9, 10, 12-14 are new, which have been fully characterized by elemental analysis, spectroscopy and X-ray crystallography. 相似文献
863.
A novel vanadium(IV) phosphite, (VO)(4)(4,4'-bpy)(2)(HPO(3))(4), was hydrothermally synthesized and characterized by single-crystal X-ray diffraction. This compound crystallizes in the monoclinic system with the space group C2/c and cell parameters a = 35.970(3) A, b = 15.9400(13) A, c = 10.7681(7) A, beta = 101.073(4) degrees, and Z = 8 with R(1) = 0.0482. The structure of the compound consists of trigonal bipyramidal [VO(4)N] and pseudopyramidal [HPO(3)] blocks, which are connected by corner-sharing, to form vanadium phosphite layers in the bc plane. These layers are further linked through 4,4'-bpy pillars, generating a 3D framework. Thermogravimetric analysis and magnetic susceptibility data for this compound are given. 相似文献
864.
The interaction of fluorocarbon containing hydrophobically modified polyelectrolyte(FMPAANa) with two kinds of nonionic surfactants(hydrogenated and fluorinated)in a semidilute (0.5wt%) aqueous solution had been studied by rheological measurements,Association behavior was found in both systems.The hydrophobic interaction of FMPAANa with fluorinated surfactant(FC171) is much stronger than that with hydrogenated surfactant(NP7.5) at low surfactoant concentrations.The interaction is strengthened by surfactants being added for the density of active junctions increased.Whereas distinct phenomena for FC171 and NP7.5 start to be found as the surfactants added over their respective certain concentration.The interaction of polyelectrolyte with fluorinated surfactant increases dramatical ly while that with hydrogenated surfactant decreases. 相似文献
865.
866.
Lin Bo Gong Shu Ling Gong Qin Zheng Xiong Li Yuan Yin Chen 《中国化学快报》2007,18(4):435-436
The reaction of 1,3-dipropyn-2-yloxycalix[4]arene with mercury(II)acetate could give mercury-containing alkynyl calixarenepolymer.The extraction behavior of 1,3-dipropyn-2-yl-oxycalix[4]arene towards mercury(II)ion was examined.When the moleratio of Hg~(2 )/calixarene was 1:1,the extractive percent can reach to 99.1%,and the extraction capacity was up to 431 mg/g.It couldalso decrease the Hg~(2 )concentration from 5 to 0.85 mg/L,which was only 17%of the national standard of effluent and satisfied thenational standard of drinking water.The extraction process included chemical reaction. 相似文献
867.
The interaction of Amido black 10B (AB) with DNA in basic medium was studied in the presence of cetyltrimethylammonium bromide (CTMAB) based on the measurements of resonance light scattering (RLS), UV–vis, CD spectra, and RLS imaging. The interaction has been proved to give a ternary complex of CTMAB–DNA–AB in Britton–Robinson buffer of pH 11.55, which exhibits strong negative Cotton effect at 233.3 nm and 642.8 nm, and strong RLS signals characterized at 469 nm. Experiments showed that the enhanced RLS intensities (ΔIRLS) against the mixture of AB and CTMAB are proportional to the concentration of fish sperm DNA (fsDNA) and calf thymus DNA (ctDNA), respectively over the range of 0.03–1.0 and 0.05–1.5 μg ml−1, with the limits of determination (3σ) of 7.3 ng ml−1 for fsDNA and 7.0 ng ml−1 for ctDNA. 相似文献
868.
Two new ent‐abietane diterpenoids, macrophynin E ( 1 ) and macrophynin F ( 2 ), and a known related ent‐abietanoid (?)‐lambertic acid ( 3 ), together with four known ent‐kauranoids, were isolated from the roots and aerial parts of Isodon macrophylla, respectively. The structures of the new compounds were elucidated on the basis of spectroscopic‐data analysis and chemical correlations. 相似文献
869.
Biosorption of metal ions with Penicillium chrysogenum 总被引:1,自引:0,他引:1
Biosorption of metal ions with Penicillium chrysogenum mycelium is described in this article. Alkaline pretreatment was used to remove proteins and nucleic acids from cells, and
this treatment increased the adsorption capacities, for Cr3+ from 18.6 mg g−1 to 27.2 mg g−1, for Ni2+ from 13.2 mg g−1 to 19.2 mg g−1, for Zn2+ from 6.8 mg g−1 to 24.5 mg g−1. The adsorption of metal ions was strongly pH dependent. The mycelium could beused for large-scale removal of Cr3+ from tannery wastewater. The results show that this inexpensive mycelium adsorbent has potential in industry because of its
high adsorption capacity. The main chelating sites are amino groups (−NH2) of chitosan in the mycelium. A new model is established, which describes the relation of adsorption of metal ions on pH
according to amino group chelating with metal ions and H+. The relative errors of simulation for Cu2+, Ni2+, Zn2+, and Cr3+ are 4.66%, 5.45%, 11.55%, and 1.69%, respectively. 相似文献
870.
采用共沉淀并加法制备了B位掺杂烧绿石型稀土复合氧化物纳米微晶Y2Sn2-xFexO7-δ(x=00~10)。制备的纳米微晶属于立方晶系,Fd3m,晶胞参数与掺杂量呈线性关系。通过Msbauer、TGDTA,气相色谱和γ射线辐照等技术研究了纳米微晶对CO的催化选择性能。结果表明,纳米微晶对CO的催化选择性明显高于一般粉料对CO的选择性;纳米微晶对CO的选择性与掺杂量有关;未辐照的纳米微晶,当掺杂量x=06时,其对CO的选择性为最高,辐照后的纳米微晶,当掺杂量x=04时,其对CO的选择性为最高 相似文献