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91.
Dr. Hoon Hyun Dr. Hideyuki Wada Dr. Kai Bao Dr. Julien Gravier Dr. Yogesh Yadav Dr. Matt Laramie Dr. Maged Henary Dr. John V. Frangioni Dr. Hak Soo Choi 《Angewandte Chemie (International ed. in English)》2014,53(40):10668-10672
The conventional method for creating targeted contrast agents is to conjugate separate targeting and fluorophore domains. A new strategy is based on the incorporation of targeting moieties into the non‐delocalized structure of pentamethine and heptamethine indocyanines. Using the known affinity of phosphonates for bone minerals in a model system, two families of bifunctional molecules that target bone without requiring a traditional bisphosphonate are synthesized. With peak fluorescence emissions at approximately 700 or 800 nm, these molecules can be used for fluorescence‐assisted resection and exploration (FLARE) dual‐channel imaging. Longitudinal FLARE studies in mice demonstrate that phosphonated near‐infrared fluorophores remain stable in bone for over five weeks, and histological analysis confirms their incorporation into the bone matrix. Taken together, a new strategy for creating ultra‐compact, targeted near‐infrared fluorophores for various bioimaging applications is described. 相似文献
92.
Dr. Hiromu Kashida Hidenori Azuma Ryoko Maruyama Dr. Yasuyuki Araki Prof. Dr. Takehiko Wada Prof. Dr. Hiroyuki Asanuma 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(28):11456-11459
Herein we report the construction of efficient light-harvesting antennae by hybridization of DNA oligonucleotides containing high densities of fluorophores into DNA junctions through d -threoninol. Six pyrene donors could be incorporated into each arm without self-quenching. A perylene acceptor was located at the center of the junction. Antenna effects of a duplex and three- to eight-way junctions were systematically compared. Six- and eight-way junctions had the highest antenna effects, and their effective absorption coefficients were 8.5 times higher than that of perylene. Interestingly, even-numbered junctions had higher efficiencies than odd-numbered junctions. Nondenaturing gel analyses and fluorescence lifetime measurements demonstrated that the strong odd–even effects were derived from differences in the stability of junctions. The results presented will guide the design of efficient artificial photosynthetic systems. 相似文献
93.
Shuntaro Matsuta Noriaki Shima Hidenao Kakehashi Akari Ishikawa Ryutaro Asai Atsushi Nitta Misato Wada Shihoko Nakano Hiroe Kamata Yoshio Nishiyama Hirohisa Nagatani Hisanori Imura Munehiro Katagi 《Journal of mass spectrometry : JMS》2020,55(9)
Various cathinone‐derived designer drugs (CATs) have recently appeared on the drug market. This study examined the mechanism for the generation of dehydrated ions for CATs during electrospray ionization collision‐induced dissociation (ESI‐CID). The generation mechanism of dehydrated ions is dependent on the amine classification in the cathinone skeleton, which is used in the identification of CATs. The two hydrogen atoms eliminated during the dehydration of cathinone (primary amine) and methcathinone (secondary amine) were determined, and the reaction mechanism was elucidated through the deuterium labeling experiments. The hydrogen atom bonded to the amine nitrogen was eliminated with the proton added during ESI, in both of the tested compounds. This provided evidence that CATs with tertiary amine structures (such as dimethylcathinone and α‐pyrrolidinophenones [α‐PPs]) do not undergo dehydration. However, it was shown that the two major tertiary amine metabolites (1‐OH and 2″‐oxo) of CATs generate dehydrated ions in ESI‐CID. The dehydration mechanisms of the metabolites of α‐pyrrolidinobutiophenone (α‐PBP) belongs to α‐PPs were also investigated. Stable‐isotope labeling showed the dehydration of the 1‐OH metabolite following a simple mechanism where the hydroxy group was eliminated together with the proton added during ESI. In contrast, the dehydration mechanism of the 2″‐oxo metabolite involved hydrogen atoms in three or more locations along with the carbonyl group oxygen, indicating that dehydration occurred via multiple mechanisms likely including the rearrangement reaction of hydrogen atoms. These findings presented herein indicate that the dehydrated ions in ESI‐CID can be used for the structural identification of CATs. 相似文献
94.
Shigeru Wada 《Macromolecular Symposia》1992,57(1):327-329
The degradation of the physical properties of polypropylene (PP) used for automotive outer trims for several years is unexpectedly small. It, therefore, can be fully anticipated that PP so used can be recycled for the same purpose or for other applications. 相似文献
95.
Masahisa Wada Takeshi Okano Junji Sugiyama Fumitaka Horii 《Cellulose (London, England)》1995,2(4):223-233
We have investigated unlignified tension wood and normally lignified wood celluloses inPopulus maximowiczii with particular reference to the composition of two crystalline phases I/I (triclinic/ monoclinic). Four independent techniques, which enable us to detect the two phases, CP/MAS13C NMR, Fourier transform infrared microscopy, selected-area electron diffraction, and X-ray diffraction were applied. Because of the low crystallinity of wood celluloses, particularly in the case of celluloses in the lignified cell wall, no single method was decisive enough to be able to determine the composition of the two phases as one can with highly crystalline materials. The I dominant structure (monoclinic crystal type) was, however, preferred for both tension and normal wood celluloses. 相似文献
96.
Tae-Ho Kim Masakazu Saito Masaya Matsuoka Shinya Tsukada Kiyohisa Wada Masakazu Anpo 《Research on Chemical Intermediates》2010,36(5):453-461
It was found that the photoelectrochemical performance and photocatalytic activity of rod-type TiO2 electrodes were affected by various post-calcination treatments, for example, calcination in NH3 or under vacuum. Post-calcination treatment in NH3 at 773 K was particularly effective in increasing the photoelectrochemical performance and photocatalytic activity of rod-type
TiO2 electrodes. A unique photoelectrochemical circuit was constructed by connecting a rod-type TiO2 electrode to a Pt electrode through a silicon solar cell in which the negative bias was applied on the rod-type TiO2 electrode. It was found that the photoelectrochemical circuit can effectively oxidize ethanethiol in water into CO2. 相似文献
97.
Controllable Electronic Structures and Photoinduced Processes of Bay‐Linked Perylenediimide Dimers and a Ferrocene‐Linked Triad
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Haruki Horinouchi Dr. Hayato Sakai Prof. Yasuyuki Araki Prof. Tomo Sakanoue Prof. Taishi Takenobu Prof. Takehiko Wada Prof. Nikolai V. Tkachenko Prof. Taku Hasobe 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(28):9631-9641
A series of perylene‐3,4,9,10‐bis(dicarboximide) (PDI) dimers linked through the bay regions was systematically synthesized to examine the electronic structures and photophysical properties in dependence on the distance and orientation between the two PDI units. The spectroscopic and electrochemical measurements suggested that the coupling value of a directly linked PDI dimer (PDI)2 is much larger than those of para‐ and meta‐phenylene‐bridged PDI dimers p‐(PDI)2 and m‐(PDI)2. The width of Davydov splitting was quantitatively evaluated to compare the coupling values between the two PDI units in these dimers by absorption spectroscopy in frozen 2‐methyl‐THF. Excimer formation of PDI dimers induced the strong fluorescence quenching and large red‐shifts. Femtosecond transient absorption revealed a broad absorption derived from an excimer in the range from about 600 nm to the near‐IR region. The rate constants of formation and decay of the excimer are strongly dependent on the coupling values. Time‐resolved measurements on ferrocene‐linked p‐(PDI)2 revealed a competition between the photoinduced processes of electron transfer and excimer formation in PhCN, which is in sharp contrast with the sole electron‐transfer process in toluene. 相似文献
98.
Masahiro Yamashita Daisuke Kawakami Satoshi Matsunaga Yoshio Nakayama Mari Sasaki Shinya Takaishi Fumiyasu Iwahori Hitoshi Miyasaka Ken‐ichi Sugiura Yoshiki Wada Hiroshi Miyamae Hiroyuki Matsuzaki Hiroshi Okamoto Hisaaki Tanaka Kazuhiro Marumoto Shin‐ichi Kuroda 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2004,116(36):4867-4871
99.
Utilization of a metalloligand, ([Cu(2,4-pydca)2(H2O)].2Et3NH) (1) (2,4-pydca = pyridine-2,4-dicarboxylate), as a building unit provides a novel porous coordination polymer, ([ZnCu(2,4-pydca)2(H2O)3(DMF)].DMF)n (2), in which the Zn(II) ion at the node of the network acts as a linker and the Cu(II) ion in the channel wall is available for guest-coordination. 相似文献
100.
Quasi-solid-state dye-sensitized solar cells using room temperature molten salts and a low molecular weight gelator 总被引:1,自引:0,他引:1
Kubo W Kitamura T Hanabusa K Wada Y Yanagida S 《Chemical communications (Cambridge, England)》2002,(4):374-375
A dye-sensitized solar cell fabricated using the room temperature molten salt, 1-hexyl-3-methylimidazolium iodide, iodine and a low molecular weight gelator as a quasisolid-state electrolyte showed a 5.0% light-to-electricity conversion efficiency under AM 1.5 irradiation, and high-temperature stability. 相似文献