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101.
102.
Eishun Tsuchida Yoshihito Osada Kei Sanada 《Journal of polymer science. Part A, Polymer chemistry》1972,10(11):3397-3404
The interaction between sodium poly(styrene sulfonate) (NaSS) and side-chain charged polycation polymer (pendent type) or main-chain charged polycation polymer (integral type) has been studied. It was found that the polyion complex (the reaction product of these polyelectrolytes) of pendent–pendent type has an equimolar composition at any mixing ratio of two component polymers. However, a polyion complex of integral–pendent type can form a water-soluble complex with a ratio of [polycation]/[polyanion] = 1/3, in addition to a complex with a equimolar composition. The mechanism of formation of this specific complex is discussed. 相似文献
103.
Okada S Okinaka K Iwawaki H Furugori M Hashimoto M Mukaide T Kamatani J Igawa S Tsuboyama A Takiguchi T Ueno K 《Dalton transactions (Cambridge, England : 2003)》2005,(9):1583-1590
This study reports substituent effects of iridium complexes with 1-phenylisoquinoline ligands. The emission spectra and phosphorescence quantum yields of the complexes differ from that of tris(1-phenylisoquinolinato-C2,N)iridium(iii)(Irpiq) depending on the substituents. The maximum emission peak, quantum yield and lifetime of those complexes ranged from 598-635 nm, 0.17-0.32 and 1.07-2.34 micros, respectively. This indicates the nature of the substituents has a significant influence on the kinetics of the excited-state decay. The substituents attached to phenyl ring have an influence on a stability of the HOMO. Furthermore, those substituents have effect on the contribution to a mixing between 3pi-pi* and (3)MLCT for the lowest excited states. Some of the complexes display the larger quantum yield than Irpiq, which has the quantum yield of 0.22. The organic light emitting diode (OLED) device based on tris [1-(4-fluoro-5-methylphenyl)isoquinolinato-C2,N]iridium(iii)(Ir4F5Mpiq) yielded high external quantum efficiency of 15.5% and a power efficiency of 12.4 lm W(-1) at a luminance of 218 cd m(-2). An emission color of the device was close to an NTSC specification with CIE chromaticity characteristics of (0.66, 0.34). 相似文献
104.
105.
Tsuboyama A Takiguchi T Okada S Osawa M Hoshino M Ueno K 《Dalton transactions (Cambridge, England : 2003)》2004,(8):1115-1116
The synthesis, structure, and photophysical properties of a new cyclometalated dinuclear iridium complex, (ppy)2Ir(mu-BPB)Ir(ppy)2 [ppy = 2-phenylpyridine, BPB = 1,4-bis(pyridin-2-yl)benzene], have been investigated. 相似文献
106.
Itaka K Kanayama N Nishiyama N Jang WD Yamasaki Y Nakamura K Kawaguchi H Kataoka K 《Journal of the American Chemical Society》2004,126(42):13612-13613
An siRNA nanocarrier formed through self-assembly of PEG-based block catiomer possessing two distinct amino groups with different pKa values in a side chain was developed. This design provided the carrier with a sufficient siRNA complexation and an assumed buffering capacity in the endosomes, allowing it to exhibit remarkable gene knockdown abilities as well as sufficient serum tolerability. 相似文献
107.
Ikeda S Sanuki R Miyachi H Miyashita H Taniguchi M Odashima K 《Journal of the American Chemical Society》2004,126(33):10331-10338
A Ni(0)/ZnCl(2) system effectively promotes the coupling of enones and alkene-tethered alkynes. In the reaction with 1,6-enynes, the oxidative cyclization of Ni(0) species on enones across the alkyne part followed by ZnCl(2)-promoted cleavage generates alkenylnickel intermediates. Subsequent migratory insertion of the tethered alkene occurs with 5-exo-cyclization. When the resulting sigma-alkylnickel intermediates have beta-hydrogen atoms, the reaction terminates by beta-hydrogen elimination to provide cyclopentane derivatives. On the other hand, a sigma-alkylnickel intermediate that does not have beta-hydrogen atoms undergoes the insertion of a second alkene unit to cause a domino effect via a three-fold C-C bond formation process with and without the cleavage of one C-C bond. 相似文献
108.
109.
The crystal structure of [{O=VV(salen)}2(mu-F)][VIVO(salen)][BF4].(CH2Cl2)x revealed a hollow cavity with a diameter of 5.3 A that penetrates through the crystal, and a remarkable cyclic chain of the [VO(salen)] unit, a motif that has never been fashioned from oxometal building blocks. These features endow the crystal with a molecular sievelike property for the rapid, reversible, and size-selective absorption of guest CH2Cl2 molecules. 相似文献
110.
Polyion complex micelles entrapping enzyme molecules in the core provide a unique reaction field inducing a remarkable elevation of enzymatic reactivity through a drastic change in the binding specificity between the enzyme and substrate. On-off switching of this enhanced effect was achieved through the destabilization of the core domain by applying a pulse electric field. 相似文献