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41.
In the present study, the effects of charge‐transfer complex formation and intramolecular fragmentation (side‐chain lactonization) in radical copolymerization of tert‐butyl vinyl ether (t‐BVE) with anhydrides of maleic (MA) and citraconic (CA) acids and the structure–thermal behavior relationships of the resulting copolymers were examined using the 1H‐NMR, FTIR, DSC, and TGA analysis methods. It was shown that copolymerization under the chosen conditions proceeded through intramolecular fragmentation with the formation of γ‐lactone units. Side‐chain fragmentation of t‐BVE–MA and t‐BVE–CA copolymers also was confirmed by TGA and DSC analysis. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2455–2463, 2006 2006 相似文献
42.
Thermal characterization of maleic anhydride‐styrene‐allyl propionate (MA‐St‐AP) terpolymer and its ester derivatives named as n‐alkyl maleate and shown as nPr MA‐St‐AP, nBu MA‐St‐AP, nPn MA‐St‐AP, and nBz MA‐St‐AP was carried out. The thermal characterization was performed using thermal analysis techniques such as TGA, DTA, DSC, and TMA. Different results were observed between the original terpolymer and its ester derivatives. Thermal stabilities of the terpolymer and its ester derivatives were compared by using various measurements plotted as TGA, DTA, DSC, and TMA curves. The increase in the alcohols' carbon numbers added to the original terpolymer results in ester derivatives with different thermal stability behavior. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 600–604, 2007 相似文献
43.
44.
Jürgen Pawlik Christian Kautz Martin Baumgarten 《Journal of Inorganic and Organometallic Polymers》1994,4(3):237-250
The use of (tetrakis(4-hexylphenyl)porphyrinato)Fe(II) in polymerization reactions with bidentate ligands such as 9,10-diisocyanoanthracene and 1,4-diisocyanobenzene led to well-defined stacked polymers1 and2 which are still soluble in common organic solvents such as chloroform, dichloromethane, and tetrahydrofurane. They have been completely characterized by1H-NMR and UV/vis spectropscopy in solution, even allowing end-group analysis for determination of the average degree of polymerization, yieldingn=10 andn=5 for1 and2, respectively. Mößbauer and IR spectroscopy further established the strong Fe-CN bonding reflected by very small isomer shifts and quadrupole splittings (E
Q0.2 mm s–1) and a large decrease in the IR stretching frequency (v
CN60 cm–1). The axially stacked polymers exhibit semiconducting properties only upon doping.Presented at the 5th International Symposium on Macromolecule-Metal Complexes (MMV), Summer 1993 in Bremen, Germany. 相似文献
45.
Yang Qin Frieder Jäkle 《Journal of Inorganic and Organometallic Polymers and Materials》2007,17(1):149-157
The binding of Lewis bases to organoboron polymeric Lewis acids has been studied and the parameters that determine the complexation
equilibrium have been investigated, which include (i) the strength of the individual Lewis acids and Lewis bases, (ii) concentration,
and (iii) temperature. While the strongly Lewis acidic borane polymers poly(4-bis(pentafluorophenyl)borylstyrene) (PS-BPf) and poly(4-(di-2-thienylboryl)styrene) (PS-BTh) form isolable complexes with strong Lewis bases such as 4-t-butylpyridine (tPy), a temperature dependent equilibrium is established with weaker bases such as THF. Similarly, the weakly Lewis acidic
boronate polymer poly(4-diethoxyborylstyrene) (PS-BOEt) undergoes a temperature dependent equilibrium with the strong Lewis base 4-dimethylaminopyridine (DMAP), while poly(4-pinacolatoborylstyrene)
(PS-BPin) does not significantly bind to pyridine bases. Decomplexation of PS-BTh·
t
Py is achieved by treatment with the stronger Lewis acid, B(C6F5)3, thereby confirming the reversible nature of the polymeric Lewis acid–base adducts.
This paper is dedicated to Professor Ian Manners in gratitude of his guidance throughout the years and recognition of his
scientific accomplishments 相似文献
46.
Preparation and characterization of multi-walled carbon nanotubes supported PtRu catalysts for proton exchange membrane fuel cells 总被引:1,自引:0,他引:1
A series of PtRu nanocomposites supported on H2O2-oxidized multi-walled carbon nanotubes (MWCNTs) were synthesized via two chemical reduction methods—one used aqueous formaldehyde (HCHO method) and the other used ethylene glycol (EG method) as the reducing agents. The effects of the solvents (water and ethylene glycol) and the surface composition of the MWCNTs on the deposition and the dispersion of the metal particles were investigated using N2 adsorption, TEM, ICP-AES, FTIR and TPD. The wetting heats of the MWCNTs in corresponding solvents were also measured. The characterizations suggest that combination of the surface chemistry of the MWCNTs with the solvents decides the deposition and the dispersion of the metal nanoparticles. These nanocomposites were evaluated as proton exchange membrane fuel cell anode catalysts for oxidation of 50 ppm CO contaminated hydrogen and compared with a commercial PtRu/C catalyst. The data reveal superior performances for the nanocomposites prepared by the EG method to those by the HCHO method and even to that for the commercial analogue. Structure–performance relationship of the nanocomposites was also studied. 相似文献
47.
Magorzata T. Kaczmarek Izabela Pospieszna-Markiewicz Maciej Kubicki Wanda Radecka-Paryzek 《Inorganic chemistry communications》2004,7(12):1247-1249
The one-step metal promoted reaction between salicylaldehyde and 4-methyl-1,3-phenylenediamine in the presence of lanthanum(III) or gadolinium(III) nitrate yields new salicylaldimine complexes containing N,N′-bis(salicylidene)-4-methyl-1,3-phenylenediamine as a result of the [2 + 1] Schiff base condensation. The crystal structure of the gadolinium complex reveals a dinuclear species with four unionized ligands coordinating in the monodentate and bridging bidentate fashion, using exclusively the oxygens as donor atoms with the nitrogen atoms not being involved in coordination. The coordination number of nine is achieved by involving three bidentate nitrate counterions in the coordination sphere. 相似文献
48.
49.
A classical ionic inorganic complex Na2[Cu(mnt)2] (mnt2− = maleonitriledithiolate = 1,2-dicyanoethylenedithiolate), that acts as a template in assembling neutral [Cu(salen)] (salen = bis(salicylidene)ethylenediamine) complexes forming a framework type arrangement, is accommodated in the channel formed in the crystal structure of a new type of host–guest compound [Cu(salen)]4 · Na2[Cu(mnt)2] (1). The non-covalent supramolecular interactions among [Cu(salen)] complexes and between [Cu(salen)] and [Cu(mnt)2]2− complexes in the crystal lattice of 1 result in weak antiferromagnetic coupling. 相似文献
50.
研究了5种二辛基二硫代磷酸稀土配合物(REDODP)对天然橡胶(NR)硫化特性、力学性能和老化性能的影响,并与二辛基二硫代磷酸钾(KDODP)和二辛基二硫代磷酸锌(ZnDODP)进行了对比。结果表明,含REDODP的NR胶料的正硫化时间介于含ZnDODP和KDODP的胶料之间,但抗返原性比KDODP的好,而与ZnDODP的相近。由于REDODP促进剂中RE是三配位,胶料中RE含量较低,降低了硫化胶的交联密度,对力学性能有一定的影响,但硫化胶老化前后拉伸强度及拉断伸长率下降幅度低于含KDODP和ZnDODP的硫化胶,表明REDODP有利于提高NR硫化胶的耐老化性能。 相似文献