共查询到20条相似文献,搜索用时 15 毫秒
1.
《Journal of Coordination Chemistry》2012,65(19):3432-3439
Thirteen new stannacyclododecane dithiocarbamate complexes have been prepared by reacting 12-chloro-12-n-butyl-1,11-dioxa-4,8-dithia-12-stannacyclododecane (1) and 12-chloro-12-n-butyl-1,4,8,11-tetrathia-12-stannacyclododecane (2) with pyrrolidine-, morpholine-, thiomorpholine-, piperidine-, piperazinebis-, and 3-pyrroline-carbodithioates, respectively, as well as with diethyl-dithiocarbamate. All complexes were characterized by elemental analyses, IR, EI-MS, and NMR (1H, 13C, and 119Sn) studies. The spectroscopic data suggest the replacement of the chlorides by the corresponding dithiocarbamates with monodentate coordination, leading to six-coordinate tin atoms in all the cases. 相似文献
2.
A new affinity adsorbent, using D-alanyl-D-alanine as ligand, has been prepared. The dipeptide immobilized on Activated CH-Sepharose
4B (D-Ala-D-Ala-AGA) bioselectively binds the glycopeptide antibiotics teicoplanin, vancomycin, ristocetin A (vancomycinlike
group of antibiotics) while it does not bind other antibiotics equally active on cell wall biosynthesis but with different
target sites, such as penicillin G, cephalosporin C, gardimycin, and bacitracin. Teicoplanin, vancomycin, and ristocetin A
have similar binding characteristics for the immobilized dipeptide, as indicated by equilibrium binding experiments. The affinity
constants of the three antibiotics for D-Ala-D-Ala-AGA is of the same order of magnitude (105 L mol-1) and the number of effective binding sites is similar for each antibiotic (6–7 μEq/mL of gel). The adsorption is biospecific
as no binding has been observed to immobilized L-alanyl-L -alanine.
D-Ala-D-Ala-AGA has been successfully used to purify teicoplanin from mixtures of different complexity and for concomitant
extraction and purification from fermentation liquors by both batch adsorption and column chromatography. The antibiotic can
be recovered from the resin in high yields by elution at pH 11. 相似文献
3.
The present work presents a study on the grafting of polyurethane onto chitosan. Prepolymers (polyurethanes) were obtained by condensation reactions between poly(ethylene glycol) of two different molar masses and isophorone diisocyanate. Characterization of graft copolymers was performed by infrared spectroscopy (IR) and 13C Nuclear Magnetic Resonance in the solid state (13C NMR). Evidences of grafting were obtained by IR from the absorbance increase of relative intensity of NH and CO bands, with respect to chitosan. The degree of NH2 substitution by urea groups observed from 0.12 to 0.59 was estimated from NMR data. The graft copolymers exhibited different solubility behavior as a function of degree of substitution, such as partial solubility, gelation or swelling in diluted acetic acid, and swelling in water, dimethylsulfoxide and acetic acid/sodium acetate. 相似文献
4.
Yan-Hong L Tong-Lai Z Jian-Guo Z Jin-Yu G Kai-Bei Y 《Molecules (Basel, Switzerland)》2005,10(8):978-989
In this paper we elected to nitrate p-xylene because this compound has only one mononitro- and trinitro- isomer. Trinitro-p-xylene was used as a starting material for the synthesis of other compounds in subsequent work. The mononitration of p-xylene can be easily carried out at 30 degrees C. Nitro-p-xylene is easily nitrated to dinitro-p-xylene at a temperature of 80 degrees C. The trinitro-p-xylene can be obtained at 120 degrees C. Single crystals of 2,3-dinitro-p-xylene and 2,3,5-trinitro-p-xylene were grown using the slow cooling method and we report the X-ray structure of the former. The thermal decomposition of the compounds was studied using differential scanning calorimetry (DSC) and thermogravimetry-derivative thermogravimetry (TG-DTG) techniques and FT-IR. The target compounds were also characterized by (1)H-NMR, (13)C-NMR and MS. 相似文献
5.
6.
Robert C. Evers 《Journal of polymer science. Part A, Polymer chemistry》1970,8(2):563-576
A series of polyiminobenzothiazoles was synthesized by the polymerization of either 2,6-dichloro- or 2,6-diphenoxybenzobisthiazole with a number of aromatic diamines. A polymer was also obtained from the self-condensation of either 2-chloro- or 2-phenoxy-6-aminobenzothiazole. The polymers were characterized by their elemental analysis and infrared spectra. Thermogravimetric analysis, differential thermal analysis, and softening under load were used to evaluate their thermal properties. The polymers were found to be light tan to brown powders which showed only slight softening below their decomposition temperatures. Onset of breakdown under thermogravimetric analysis in a nitrogen atmosphere generally occurred at 375–400°C. The polymers were sparingly soluble in organic solvents and had inherent viscosities in the range of 0.11–0.55. 相似文献
7.
R. E. Singler G. L. Hagnauer N. S. Schneider B. R. Laliberte R. E. Sacher R. W. Matton 《Journal of polymer science. Part A, Polymer chemistry》1974,12(2):433-444
The synthesis, dilute solution characterization, and thermal analysis of seven polyaryloxyphosphazenes are described. Synthesis is accomplished by the ring-opening polymerization of hexachlorocyclotriphosphazene at 245°C, followed by reaction of polydichlorophosphazene with sodium aryloxide salts in solution at 115°C. Polymers prepared and characterized have the general structure [(ArO)2PN]n, with Ar = C6H5, m- and p-CH3C6H4, m- and p-ClC6H4, p-C2H5C6H4, or p-CH3OC6H4. Elemental and infrared analyses show these polymers are essentially free of reactive chlorine sites. All the polymers displayed high intrinsic viscosities [η] > 1 dl/g, in tetrahydrofuran or chloroform. Closer examination of the dilute solution properties of two polyaryloxyphosphazenes revealed high molecular weights (M?w> 6 × 105) and broad molecular weight distributions (M?w/M?n > 4.7). The experimental values for the Z-average radii of gyration, 〈S2〉z1/2, characterized at near theta conditions, are larger than the calculated values for a freely rotating chain, which suggests that these polymers are relatively linear and not highly branched. Thermal analysis revealed second-order glass transitions between ?37 and +13°C and first-order endothermic transitions between 43 and 160°C for the different polymers. Although crystalline structure can persist above this first-order transition, this temperature can be regarded as a melting temperature or softening temperature at which films can be molded. Decomposition temperatures, measured in argon and oxygen, ranged from 250°C to 400°C. 相似文献
8.
三羟甲基烷烃是用于醇酸树脂、聚氨酯树脂、表面活性剂、合成润滑油等的原料[1-3].三羟甲基十一烷(化学结构见图1)作为三羟甲基烷烃中直碳链最长的一员,不仅具有亲水性(分子中含三个亲水基),而且具有疏水性(含一个长直碳链亲油基),因此可用作表面活性剂.不仅如此,与同样用作乳化剂的一般高级脂肪醇(如十六烷醇)相比,可以在化妆品用的乳液中加入三羟甲基十一烷作乳化剂,以降低乳液的黏度,防止乳液中由于大量加入高级脂肪醇而导致产品黏度过高以至不能在皮肤上被充分涂抹开的状况发生[4].为制备智能芳香缓释型聚氨酯微胶囊壳材[5],需要设计聚氨酯的分子结构中含有能与相变石腊和油溶性香料有良好相容性的疏水链(三羟甲基十一烷与六亚甲基二异氰酸酯的加成物).因此,本文合成并表征了三羟甲基十一烷. 相似文献
9.
Plévert J Sanchez-Smith R Gentz TM Li H Groy TL Yaghi OM O'Keeffe M 《Inorganic chemistry》2003,42(19):5954-5959
Six new zirconogermanates have been prepared under hydrothermal conditions using amines as bases. There are four new structure types (ASU-n) with a common motif of ZrGe(5). ASU-23 is a layered structure: ZrGe(3)O(8)(OH)F.[C(10)H(26)N(4)].H(2)O, space group P2(1)/n, a = 6.7957(8) A, b = 12.700(1) A, c = 24.293(3) A, beta = 97.936(2) degrees, V = 2076.4(4) A(3). ASU-24 is a pillared layered structure: Zr(3)Ge(6)O(18)(OH(2),F)(4)F(2).[C(6)H(18)N(2)].[C(6)H(17)N(2)](2).2H(2)O, space group P2(1)/n, a = 7.4249(3) A, b = 25.198(1) A, c = 11.3483(5) A, beta = 90.995(1) degrees, V = 2122.9(2) A(3). This material has the lowest framework density (FD) of any oxide material that we are aware of (FD = 8.48 metal atoms/nm(3)). Two other materials form three-dimensional open-frameworks, ASU-25: ZrGe(3)O(9).[C(3)H(12)N(2)], space group P112(1)/a, a = 13.1994(4) A, b = 7.6828(2) A, c = 11.2373(3) A, gamma = 91.233(3) degrees, V = 1139.29(5) A(3). The other is ASU-26: ZrGe(3)O(9).[C(2)H(10)N(2)], space group Pn, a = 13.7611(3) A, b = 7.7294(2) A, c = 11.2331(3) A, beta = 104.793(1) degrees, V = 1155.21(4) A(3). ASU-25 is related to the mineral umbite K(2)ZrSi(3)O(9).H(2)O. The germanium equivalent has been prepared through the inorganic route: K(2)ZrGe(3)O(9).H(2)O, space group P2(1)2(1)2(1), a = 13.6432(6) A, b = 7.4256(3) A, c = 10.3973(4) A, V = 1053.33(8) A(3). The structural relationships between ASU-25 and its inorganic counterpart are described. The thermal decomposition of the germanium umbite generated the cyclic trigermanate K(2)ZrGe(3)O(9), analogue of the mineral wadeite, crystallizing in the orthorhombic system, a = 7.076 A, b = 12.123 A, c = 10.451 A, V = 904.5 A(3). 相似文献
10.
Žaneta Mesíková Petra Šulcová M. Trojan 《Journal of Thermal Analysis and Calorimetry》2007,88(1):103-106
Phosphates belong to the extensive group
of inorganic pigments that are very often used in industry of plastics and
anticorrosive paints. Also, the powders of newberyite MgHPO4·3H2O
and α-pyrophosphate Mg2P2O7
can find the usage in this field. Thus, these compounds were the centre of
our attention. Newberyite and α-pyrophosphate were synthesized by the
method of gelling. Impact of various ways of synthesis, especially reaction
conditions, on the structural, thermal, physical and optical properties was
investigated. α-pyrophosphate was synthesized by the thermal decomposition
of newberyite at temperature around 500°C. Both powders are white color,
but the newberyite is the whitest one. The reaction pH particularly affected
the particle size distribution and optical properties. 相似文献
11.
Dibenzodioxadiselenafulvalene (DBOSF) was prepared and the cis and trans isomers were separated. X-ray crystallographic analysis revealed the presence of Se- - -H and O- - -H hydrogen bonds in both crystals. The electrochemical properties of cis- and trans-DBOSFs together with dibenzotetraoxafulvalene (DBTOF) and cis- and trans-dibenzodioxadithiafulvalenes were investigated by means of cyclic voltammetry and DFT calculation. The electron-donating ability and the stability of oxidized forms of DBOSFs are improved compared with those of DBTOF. 相似文献
12.
Yamada H Kuzuhara D Takahashi T Shimizu Y Uota K Okujima T Uno H Ono N 《Organic letters》2008,10(14):2947-2950
Linearly pi-expanded novel tetraanthroporphyrins with and without aromatic rings at the meso-positions were prepared quantitatively for the first time from the corresponding precursors by a retro-Diels-Alder reaction. 相似文献
13.
The synthesis of several meso-triaryl-subporphyrins, based on utilizing tripyrrolylborane as a precursor in a reaction with arylaldehydes (where aryl = phenyl, 4- and 3-pyridyl, tolyl, 4-methoxyphenyl, and 4-(trifluoromethyl)phenyl) under reflux in propionic acid, is reported. All of the compounds have been successfully characterized by 1H-, 13C-, and 13C-1H 2D NMR, electronic absorption, magnetic circular dichroism (MCD), IR, and fluorescence spectroscopy, together with cyclic (CV) and differential pulse (DPV) voltammetry. The X-ray structure of tris{(trifluoromethyl)phenyl}subporphyrin was found to be slightly domed and similar to that of the recently reported hexaethylsubtriazaporphyrin (Inorg. Chem. 2006, 45, 6148). The electronic absorption spectra of all of the subporphyrins contain intense Soret bands in the 370-380 nm region and weaker Q bands in the 420-550 nm region, which are at shorter wavelengths than those observed (at ca. 400-420 nm and ca. 450-650 nm, respectively) for tetrapyrrole porphyrins. The intensity of the Q00 band decreases as the meso-aryl groups become more electron withdrawing. These characteristics can be rationalized by using Gouterman's four-orbital model as a conceptual framework. The MCD bands observed in the Q band region of the subporphyrins (subPs) spectra consistently show a -ve/+ve intensity pattern in ascending energy, while, in contrast, the sign sequence of the bands observed in the Soret band region change dramatically depending on the nature of the aryl groups: from +ve/-ve in the case of the electron withdrawing 4-pyridyl, 4-(trifluoromethyl)phenyl and 3-pyridyl groups to -ve only for phenyl and -ve/+ve for the electron donating 4-tolyl and 4-methoxyphenyl groups. S1 fluorescence emission was observed in the 490-620 nm region. The quantum yields (phiF) in benzene (phiF = 0.10-0.12) are similar to that of metal-free tetraphenylporphyrin (H2TPP) (phiF = 0.11) but are somewhat lower in the case of ethanol (phiF = 0.06-0.07) due to the higher polarity. The redox potential differences observed between the first oxidation and reduction steps are in the 2.52-2.64 V range, which is larger than that of normal porphyrins (ca. 2.25 V). Molecular orbital (MO) calculations of these compounds help to provide an enhanced understanding of the spectroscopic and electrochemical properties. A byproduct of the synthesis was characterized using X-ray crystallography and a range of spectroscopic techniques. A subporphyrin mu-oxo dimer was prepared and characterized. 相似文献
14.
15.
Jacob John Jian Tang Zhihong Yang Mrinal Bhattacharya 《Journal of polymer science. Part A, Polymer chemistry》1997,35(6):1139-1148
Polycaprolactone-graft-maleic anhydride (PCL-g-MA) copolymer was prepared by grafting maleic anhydride onto PCL in a batch mixer and in an extruder using dicumyl peroxide as the initiator. The graft content was determined with the volumetric method by converting the anhydride functions to acid groups and then titrating with ethanolic potassium hydroxide. The grafted polymer was extracted with xylene to remove any unreacted monomer before the estimation step. The effect of temperature and the various concentrations of the initiator and monomer used for the grafting reaction were investigated. The presence of residual initiator in the reaction product was checked using thin-layer chromatography. Molecular weight determination was carried out for the pure and grafted polymer using gel permeation chromatography to determine if chain scission was present. Results indicate that maleic anhydride is grafted onto PCL using free radical initiators. The grafting reaction was confirmed by FTIR and NMR techniques. FTIR spectra showed absorption bands around 1785 and 1858 cm−1. NMR spectra gave signals for methine proton at 3.47 ppm. For a given peroxide level, a higher temperature or residence (reaction) time gave higher percentage of grafted MA. There was an optimum temperature and initiator concentration after which the percentage of MA grafted on PCL decreased. The number-average molecular weight, tensile strength, and the percent elongation of PCL-g-MA were comparable to those of PCL before grafting. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 1139–1148, 1997 相似文献
16.
本文提出了一种在固态条件下,通过磷酸(5 mol%)催化半乳糖与葡聚糖共聚合成了半乳糖基葡聚糖的方法。采用1H NMR确定了不同条件下产物的摩尔取代度,发现当投料比为2:1,反应时间为9h,反应温度为110℃时,MS最大为0.43。还通过凝胶渗透色谱考察了不同反应时间条件下产物分子量,发现随反应时间延长,分子量逐步减小。最后使用甲基化分析法确定了MS=0.27的半乳糖基葡聚糖糖单元连接结构,发现半乳糖基葡聚糖的主链仍然由(1→6)-连接的葡萄糖组成,支化度为11.5%,其中位于主链糖单元C3的支链比例最大。支链半乳糖均为线型连接,并且其中(1→6)-连接比例最大,平均链长约为3个糖单元。 相似文献
17.
18.
The efficient procedure to prepare novel water-soluble O-succinyl-chitosan was established by using one three-step reaction. Phthaloyl group was firstly chosen as the protection group for the amino group of chitosan, and O-succinylation was then completed. Protection group was removed finally by using hydrazine hydrate. The chemical structure of the modified chitosan was characterized by FTIR, 1H-NMR, 13C-NMR and elemental analysis. Some physical properties were analyzed by X-ray diffraction, differential scanning calorimetry (DSC), thermogravimetry (TG) and solubility test. It indicates that after O-succinylation, the modified chitosan shows much better solubility in water. The study of enzymatic degradation showed that the O-succinyl-chitosan was of low susceptibility to lysozyme. O-succinylation-chitosan is a useful intermediate, which permits further chemical modification for amino group and may be have potential applications in biomedical system. 相似文献
19.
20.
James F. Dezern 《Journal of polymer science. Part A, Polymer chemistry》1988,26(8):2157-2169
A series of thermally-stable, tough, linear polyimides containing amide linkages were prepared. These materials have potential as high temperature films and coatings as well as matrix resins in graphite reinforced structures. The new polyamide-imides were prepared by reacting a group of isomers of diaminobenzanilide (DABA) with 3,3′,4,4′-benzophenonetetracarboxylic dianhydride (BTDA) to form the polyamide-acid with subsequent thermal conversion to the polyamide-imide (PAI). Four polymers were synthesized from unsubstituted amide diamines and two others from N-substituted amide diamines. The properties of these polyamide-imides were compared to those of the polyimide of benzophenonetetracarboxylic dianhydride/3,3′-diaminobenzophenone (LARC–TPI) because their structures are similar, except for the presence of the more flexible amide linkages. These polymers exhibited high inherent viscosities and glass transition temperatures. They were made into tough, flexible films which showed good thermal stability and good resistance to organic solvents. Mechanical properties of the PAI films were better than those of LARC–TPI. Films of the 4,4′-isomer polyamide-imide exhibited an exceptionally high modulus and toughness during impact evaluation. 相似文献