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排序方式: 共有146条查询结果,搜索用时 31 毫秒
81.
Naoki Yokoyama Nobuaki Tanaka Natsumi Fujimoto Dr. Rika Tanaka Prof. Dr. Shuichi Suzuki Prof. Daisuke Shiomi Prof. Dr. Kazunobu Sato Prof. Dr. Takeji Takui Prof. Dr. Masatoshi Kozaki Prof. Dr. Keiji Okada 《化学:亚洲杂志》2021,16(1):72-79
A nitronyl nitroxide unit ( NN ) was linked with a triphenylamine-based condensed polycyclic skeleton DOTT to form a radical substituted donor NN - DOTT . X-ray crystal structure analysis demonstrated a flat bowl shape of the DOTT unit. EPR spectra showed the localization of electron spin on the NN unit. Chemical oxidation of the DOTT unit produced radical-substituted radical cation salts NN - DOTT + ⋅ SbF6− and NN - DOTT + ⋅ FeBr4− that are stable under ambient conditions. The magnetic behavior of NN - DOTT + ⋅ SbF6− is characterized by the strong intramolecular ferromagnetic interaction between NN and DOTT +. The X-ray structural analysis of NN - DOTT + ⋅ FeBr4− shows planar structure of DOTT and 1D mixed-stack column of NN-DOTT + and FeBr4−. Magnetic measurements established that NN - DOTT + ⋅ FeBr4− undergoes magnetic phase transition into a weak ferromagnet at 7 K. 相似文献
82.
A stable guanine-substituted nitronyl nitroxide radical 1 has been synthesized and characterized. The single-crystal structure analyses and magnetic susceptibility measurements exhibit a one-dimensional architecture of guanine base resulting from carbonyl-amino hydrogen bonds in the solid state, giving a 1D ferromagnetic chain of the radical moieties. 相似文献
83.
Murata T Morita Y Yakiyama Y Nishimura Y Ise T Shiomi D Sato K Takui T Nakasuji K 《Chemical communications (Cambridge, England)》2007,(39):4009-4011
The reaction between an imidazole-functionalized EDT-TTF and F(4)TCNQ produced a zwitterionic pi-radical, which formed a self-assembled structure by the cooperation of hydrogen-bonds and multiple S...S interactions and exhibited three-step oxidation processes and a high electrical conductivity as a single-component organic molecule. 相似文献
84.
Kubo T Shimizu A Uruichi M Yakushi K Nakano M Shiomi D Sato K Takui T Morita Y Nakasuji K 《Organic letters》2007,9(1):81-84
[reaction: see text] A new Kekulé polycyclic hydrocarbon with a singlet biradical index of 50% was synthesized. The singlet biradical character was assessed with UV and 1H-NMR spectroscopy, cyclic voltammetry, SQUID magnetic susceptibility measurement, and quantum chemical calculations. 相似文献
85.
Kobayashi T Takenaka M Saijo K Hashimoto T 《Journal of colloid and interface science》2003,262(2):456-465
We investigated the self-assembling structure of the 1,3:2,4-bis-O-(p-methylbenzylidene)-D-sorbitol (PDTS)/n-dibutylphthalate (DBP) system in the parameter space of temperature T and solute concentration Phi(PDTS). Optical microscopic studies revealed that the phase diagram can be divided into four regions. In region I at high T the system is a homogeneous solution. In region II at lower T and low Phi(PDTS), the system still has fluidity but has microgels having spherulitic texture of PDTS crystallites. Regions III and IV at even lower T but higher Phi(PDTS) are in a gel state. In region III, the PDTS forms volume-filling spherulites due to the solid-liquid phase transition of the saturated PDTS solutions. In region IV at the lowest T, both the liquid-liquid phase-separation process and the solid-liquid transition of the PDTS are involved in the self-assembling processes. In this region a bicontinuous phase-separated structure is first formed by liquid-liquid phase separation via spinodal decomposition (SD). The subsequent solid-liquid transition of the PDTS in the PDTS-rich region forms percolating crystalline fibrils rather than spherulites. The formation of the crystalline fibrils pins further growth of the bicontinuous structure via SD. 相似文献
86.
Suzuki S Fukui K Fuyuhiro A Sato K Takui T Nakasuji K Morita Y 《Organic letters》2010,12(21):5036-5039
Symmetric hexaazaphenalenes (R = phenyl and tert-butyl) have been synthesized by one-pot condensations of corresponding amidine hydrochlorides with tricyanomethanide. The hexaazaphenalenes are linked with each other by a N-H···N hydrogen-bonding interaction in the crystalline states. Interestingly, a planar and achiral tert-butylated derivative was crystallized in a chiral space group with assembly of one-handed helical hydrogen-bonded chains. Hexaazaphenalenyl anions were isolated as air- and water-stable tetraethyl ammonium salts. 相似文献
87.
88.
Takatoshi Sawai Kazunobu Sato Daisuke Shiomi Kazuo Toyota Qi Wang Jia-Song Wang Yong Li Guo-Shi Wu Takeji Takui 《Applied magnetic resonance》2011,41(2-4):337-352
A calix[4]arene-based biradical with two tert-butyl nitroxide radicals and a monoradical derived from the biradical have been studied by continuous-wave electron spin resonance (CW-ESR) and pulse-ESR-based hyperfine sublevel correlation (HYSCORE) spectroscopy. The two nitroxide radical sites antiferromagnetically interact with each other, generating a thermally accessible triplet state located 4?cm?1 above the singlet ground state. The present fine-structure and hyperfine spectral simulation for the spin Hamiltonian parameters of the biradical is sensitive to the local molecular structure at the spin-bearing site, illustrating a salient electronic structure of the radical sites with the ??-orbitals on the nitrogen (and oxygen) atoms cross-facing each other. The derived structure contrasts with the molecular structure determined by an X-ray crystal analysis for the hydroxylamine precursor of the biradical. The distance between the two midpoints of the nitrogen?Coxygen bonds at the radical sites is by 0.234?nm longer than the one (=0.314?nm) of the two hydroxyl groups of the precursor determined by the X-ray analysis. The lack of intramolecular hydrogen bonds between the nitrogen and hydrogen of the hydroxyl groups, caused by the oxidation of the hydroxyamino precursor, gives rise to such a sizable increase in the distance between the radical sites. The HYSCORE experiments gave a direct evidence of the local molecular structure of the radical site of the partially oxidized monoradical. The experimentally derived molecular structures of both the bi-, monoradicals and the precursor are in good agreement with those obtained by density functional theory calculations. 相似文献
89.
Takeji Takamura‐Enya Masanobu Kawanishi Takashi Yagi Yoshiharu Hisamatsu 《化学:亚洲杂志》2007,2(9):1174-1185
3‐Nitrobenzanthrone is a powerful bacterial mutagen and carcinogen to mammals. To obtain precise information on DNA‐adduct formation by 3‐nitrobenzanthrone, a number of DNA adducts, including N‐(2′‐deoxyguanosin‐8‐yl)‐3‐aminobenzanthrone ( 13 a ), 2‐(2′‐deoxyguanosin‐N2‐yl)‐3‐aminobenzanthrone ( 14 a ), N‐(2′‐deoxyadenosin‐8‐yl)‐3‐aminobenzanthrone ( 15 a ), 2‐(2′‐deoxyadenosin‐N6‐yl)‐3‐aminobenzanthrone ( 16 a ), and their N‐acetylated counterparts 13 b , 14 b , 15 b , and 16 b were synthesized by palladium‐catalyzed aryl amination of the corresponding nucleoside and bromobenzanthrone derivatives. Among these DNA adducts, DNA adducts 13 a , 13 b , 14 a , 14 b , and 16 a were identified in the reaction mixture of nucleosides (2′‐deoxyguanosine, 2′‐deoxyadenosine, or DNA) with N‐acetoxy‐3‐aminobenzanthrone or N‐acetyl‐N‐acetoxy‐3‐aminobenzanthrone, both of which are recognized as activated metabolites of 3‐nitrobenzanthrone. The formation of these multiple DNA adducts may help explain the potent mutacarcinogenicity of 3‐nitrobenzanthrone. 相似文献