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1 phyrins, a cobalt porphyrin, and a ferrocene-zinc porphyrin.
2 T)(singlet) = 0.83) creating singlet excited zinc porphyrin.
3 e-monoimide accessory pigments attached to a zinc porphyrin.
4 as capable of reacting with the photoexcited zinc porphyrin.
5 d to prepare several arrays of free base and zinc porphyrins.
6 c dipalladium complexes and tetracarboxylate zinc porphyrins.
7 ordination of guest functional groups to the zinc porphyrins.
10 ransmission element consists of one or three zinc porphyrins affording short or long wires, respectiv
12 eptor molecular dyads were constructed using zinc porphyrin and free base porphyrin (Zn(i + 2)-Zn(i +
13 ace interactions between the singlet excited zinc porphyrin and the C(60) moiety in the "tail-off" fo
14 to be (0.8 ns)(-1) for diphenylethyne-linked zinc porphyrins and increases only slightly to (0.6 ns)(
15 he electron donor was the excited state of a zinc porphyrin, and the acceptors were a series of size-
16 xad is dissolved in an organic solvent, five zinc porphyrin antenna moieties absorb light, exchange e
21 r ((n,m) = (6,5) and (7,6)) and free-base or zinc porphyrin bearing peripheral positive charges ((TMP
22 gh potential donor-acceptor dyad composed of zinc porphyrin bearing three meso-pentafluorophenyl subs
24 the zinc porphyrin monomers to afford a bis(zinc porphyrin) bearing one phthalonitrile group and one
27 e show that pseudo-octahedral six-coordinate zinc porphyrin complexes can also be formed in solution,
28 We have used the formation of six-coordinate zinc porphyrin complexes to achieve the template-directe
33 boron dipyrrin moiety in the boron dipyrrin-zinc porphyrin dyad resulted in efficient energy transfe
34 rin architectures, a p-diphenylethyne-linked zinc porphyrin dyad was prepared wherein one porphyrin b
36 ronic communication in diphenylethyne-linked zinc-porphyrin dyads has been investigated by a novel mo
39 he redox-active molecules include ferrocene, zinc porphyrin, ferrocene-zinc porphyrin, magnesium phth
43 t conjugates are then complexed with dimeric zinc porphyrin host 2 giving rise to 1:1 host/guest sand
46 separation via the singlet excited states of zinc porphyrin in the studied dyads is also confirmed by
47 ch other via p-phenylene linkers whereas the zinc porphyrins in each array are attached to the core f
48 te neutralization on the conformation of the zinc-porphyrin in the Mb heme pocket has been studied by
49 ge-separation ET from a photoexcited singlet zinc porphyrin incorporated within Mb to the heme of b(5
50 dies of the photodynamics of dyads wherein a zinc porphyrin is electrochemically oxidized and the att
52 ticomponent self-assembled system based on a zinc porphyrin macrocyclic compound, a bidentate ligand
53 include ferrocene, zinc porphyrin, ferrocene-zinc porphyrin, magnesium phthalocyanine, and triple-dec
55 on, (2) oxidative, meso,meso coupling of the zinc porphyrin monomers to afford a bis(zinc porphyrin)
56 localization is investigated in rigid linear zinc porphyrin oligomers as a function of interporphyrin
57 his strategy has been realized using tin and zinc porphyrin oligomers as the molecular building block
58 ry on triplet state delocalization in linear zinc porphyrin oligomers is explored by electron paramag
60 virus scaffold to mediate the co-assembly of zinc porphyrins (photosensitizer) and iridium oxide hydr
63 constants for a family of 96 closely related zinc porphyrin-pyridine ligand complexes have been measu
65 orming the supramolecular triad, the excited zinc porphyrin resulted in efficient electron transfer t
70 suppress the dye aggregation for a push-pull zinc porphyrin, the PSSC achieved a record 12.3% in 2011
72 minantly (>or=90%) by energy transfer to the zinc porphyrin to form the excited zinc porphyrin (Zn),
73 while the electron transfer from the excited zinc porphyrin to fullerene mimics the primary events of
77 study of complexes formed between a dimeric zinc porphyrin tweezer (host) and chiral monoalcohols an
78 round-state hole transfer between equivalent zinc porphyrins using electron paramagnetic resonance te
80 of PSSC was reported until 2005; beta-linked zinc porphyrins were then reported to show promising dev
84 of hole transfer between inequivalent sites [zinc porphyrin (Zn) and free base porphyrin (Fb)] give a
85 er to the zinc porphyrin to form the excited zinc porphyrin (Zn), which has excited-state characteris
86 henylbutadiyne-linked dyads comprised of two zinc porphyrins (Zn-pbp-Zn), two magnesium porphyrins (M
88 sembled single-walled carbon nanotube (SWNT)/zinc porphyrin (ZnP) hybrids utilizing (7,6)- and (6,5)-
89 phyrin arrays consisting of three peripheral Zinc porphyrins (ZnPs) and a central free base porphyrin
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