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1 on oxidation of the phenol by intramolecular photoinduced electron transfer.
2 the associated nanoparticles on the basis of photoinduced electron transfer.
3 ntegrate singlet-singlet energy transfer and photoinduced electron transfer.
4 reas its betaine isomer strongly quenches by photoinduced electron transfer.
5 g (1)DTEc-P-C(60) and precluding significant photoinduced electron transfer.
6 irs cyclobutylpyrimidine dimers by ultrafast photoinduced electron transfer.
7 a decrease in the efficiency of collisional photoinduced electron transfer.
8 n the direction opposite that of the initial photoinduced electron transfer.
9 PY-ATP) was quenched by Fe(III) ions through photoinduced electron transfer.
10 ryl moiety to reduce the process of acceptor photoinduced electron transfer.
11 h dielectric constants (DMF), most likely by photoinduced electron transfer.
13 sized and investigated in order to elucidate photoinduced electron transfer and hole migration mechan
14 ta rule out substrate activation by means of photoinduced electron transfer and instead support a mec
16 nceptual analogies between bridge effects in photoinduced electron transfer and optical intervalence
17 moiety, distinctly rectify both the forward photoinduced electron transfer and the subsequent charge
18 generated during pyrimidine dimer repair by photoinduced electron transfer, and it has been suggeste
20 earch to be able to study photocatalysis and photoinduced electron transfer as unifying themes that u
25 vibrational excitation of the bridge changes photoinduced electron transfer between donor (dimethylan
26 hat after photoexcitation of the donor HBC a photoinduced electron transfer between HBC and PDI can o
27 strate that SF competes with the traditional photoinduced electron transfer between pentacene and C60
28 x)/lambda(em) = 490 nm/510 nm) suggests that photoinduced electron transfer between the catechol and
29 robe fluorescence is achieved through unique photoinduced electron transfer between the naphthalimide
30 relationships are consistent with control of photoinduced electron transfer by Marcus-like excess fre
31 has been established that the first step of photoinduced electron transfer can be fast, of order 100
32 ith cationic fullerene derivatives to create photoinduced electron-transfer cascades that lead to exc
36 We show that these sites can be revealed by photoinduced electron transfer dissociation, which produ
37 complex was found to improve the rate of the photoinduced electron transfer due to the favorable stru
39 gh an efficient photochemical route requires photoinduced electron transfer (ET) from a light harvest
40 dynamics (NAMD) simulation of the ultrafast photoinduced electron transfer (ET) from a PbSe quantum
43 redox changes can be efficiently achieved by photoinduced electron transfer (ET) through a series of
45 f this complex with the acid to suppress the photoinduced electron-transfer fluorescent quenching cau
46 The optical sensor is based on a novel PET (photoinduced electron transfer) fluoroionophore immobili
48 pairs cyclobutylpyrimidine dimers (CPDs) via photoinduced electron transfer from a reduced flavin ade
49 that employs a photochromic moiety to direct photoinduced electron transfer from an excited state don
51 ransfer mechanism from Hb/AuNCs to Cyt c and photoinduced electron transfer from DNA/AgNCs to the apt
52 gy calculations suggested the possibility of photoinduced electron transfer from excited metal-quinol
54 Taken together, the data are consistent with photoinduced electron transfer from reduced FAD to subst
55 dynamics of free carrier formation following photoinduced electron transfer from the conjugated polym
56 e site and the 6-4PP, induced by the initial photoinduced electron transfer from the excited flavin c
58 solved spectroscopy experiments demonstrated photoinduced electron transfer from the graphene to the
59 PM labels completely quenched, presumably by photoinduced electron transfer from the neighboring Trp-
60 macrocycle in 2-methyltetrahydrofuran reveal photoinduced electron transfer from the porphyrin first
61 communication was observed through efficient photoinduced electron transfer from the ruthenocene unit
62 uenching of the fluorescence is explained by photoinduced electron transfer from the tertiary amine t
66 s of photocatalysis are discussed, including photoinduced electron transfer, hydrogen atom transfer,
69 Since the discovery a decade ago of rapid photoinduced electron transfer in DNA over a distance >4
76 Here we report spectroscopic measurements of photoinduced electron transfer in synthetic DNA that yie
78 ghly efficient energy transfer and ultrafast photoinduced electron transfer in well-defined multichro
79 The photochemical mechanisms examined are photoinduced electron transfer, internal charge transfer
80 the phenomenon of fluorescence quenching by photoinduced electron transfer into the isolated NTD of
82 Density functional theory studies validate a photoinduced electron transfer intramolecular switching
84 (60)) triad molecule in which intramolecular photoinduced electron transfer is controlled by the phot
88 sible photonically controlled intramolecular photoinduced electron transfer may eventually be useful
90 e reveal the existence of a new, low-energy, photoinduced electron-transfer mechanism in molecules he
91 to be suitable for the preparation of on/off photoinduced electron transfer modulated fluorescent sen
92 inated conditions, where the primary step of photoinduced electron transfer obeys to Hammett linear f
93 pectra of these hairpins established that no photoinduced electron transfer occurs for a hairpin that
94 ity functional theory, we establish that the photoinduced electron transfer occurs several times fast
96 ion center complex has been constructed, and photoinduced electron transfer originating in this supra
97 emphasis on differences between thermal and photoinduced electron transfer, oxidative and reductive
98 xchange is an effective model to rationalize photoinduced electron transfer, particularly when molecu
99 Rhodamine Voltage Reporters, or RhoVRs, use photoinduced electron transfer (PeT) as a trigger for vo
100 and theoretical studies points to a role for photoinduced electron transfer (PET) between a highly co
101 uence of the thermodynamic driving force for photoinduced electron transfer (PET) between single-wall
102 , which is mainly governed by changes in the photoinduced electron transfer (PET) driving force betwe
103 SB] complex to its protein inhibitor form by photoinduced electron transfer (PET) from a colloidal Pb
104 ATP fluorescence resulting from an oxidative-photoinduced electron transfer (PET) from the BODIPY-ATP
107 lacement of the internal charge transfer and photoinduced electron transfer (PET) modulators on the s
109 ere we reported the development of the first photoinduced electron transfer (PeT) probe (1) to direct
112 n(2+) cation to the sensor, which inhibits a photoinduced electron transfer (PET) quenching pathway.
113 n(2+) cation to the sensor, which inhibits a photoinduced electron transfer (PET) quenching pathway.
114 QMeNN, whose fluorescence is deactivated by photoinduced electron transfer (PeT) quenching that resu
115 sensors has been attributed to some form of photoinduced electron transfer (PET) quenching, which is
120 er(I)-responsive fluorescent probes based on photoinduced electron transfer (PET) switching consisten
121 oltage with high speed and sensitivity using photoinduced electron transfer (PeT) through a conjugate
122 extension to modular switch systems based on photoinduced electron transfer (PET) towards the emulati
123 IR voltage sensitive dyes that make use of a photoinduced electron transfer (PeT) trigger for optical
124 l reconfiguration dynamics of the chain, and photoinduced electron transfer (PET), a contact-based me
125 ate locally excited triplet states by way of photoinduced electron transfer (PeT), followed by recomb
127 electron affinity material (acceptor) [i.e., photoinduced electron transfer (PET), which we term Chan
128 The dye/enzyme hybrids are composed of a photoinduced electron transfer (PeT)-based fluorescent v
129 2]pseudorotaxane complex with an interrupted photoinduced electron transfer (PET)-coupled fluorescenc
131 This deoxygenation is accomplished via a photoinduced electron-transfer (PET) mechanism using car
133 8-crown-6 derivatives perform as fluorescent photoinduced electron-transfer (PET) sensors with very s
136 catalyst system is achieved by a consecutive photoinduced electron transfer process (conPET) and allo
137 dyads is associated with an extremely rapid photoinduced electron-transfer process, k(ET) approximat
140 Only in the latter case does a cascade of photoinduced electron transfer processes afford the PTZP
141 ies suitable for cascade energy transfer and photoinduced electron transfer processes in appropriate
142 c systems and in chemical systems capable of photoinduced electron transfer processes in general.
143 ical reactions, particularly those involving photoinduced electron transfer processes, establish a su
144 lecules to studies in recent years involving photoinduced electron-transfer processes occurring in na
145 Described here is a previously unreported photoinduced electron-transfer-quenched probe (HMBQ-Nap
146 t absorption spectroscopy to investigate the photoinduced electron transfer rates, which are also ver
148 ion, 2J, in a radical ion pair produced by a photoinduced electron transfer reaction can provide a di
149 the radical pair (T)[AQDS(3-*) Trp(*)] by a photoinduced electron transfer reaction from tryptophan
150 ) with zinc(II) ions allowed us to study the photoinduced electron-transfer reaction (3)Zncyt c(6) +
152 the range of 2.5-20.0 mM) on the kinetics of photoinduced electron-transfer reaction 3Zncyt/pc(II) --
153 (in the range 2.5-100 mM) on the kinetics of photoinduced electron-transfer reaction 3Zncyt/pc(II)-->
154 Laser flash photolysis is used to study the photoinduced electron-transfer reaction cyt(III)//pc(II)
156 gates, and sequence defined polymers through photoinduced electron transfer reactions are also invest
157 ount of the fundamentals and applications of photoinduced electron transfer reactions in polymer synt
158 diffusion free, rate constant of bimolecular photoinduced electron transfer reactions, fluorescence q
163 In this paper, we have investigated the photoinduced electron-transfer reactions of zinc-substit
164 s the synthesis, photophysical behavior, and photoinduced electron-transfer reactivity of multichromo
165 ence quenching was attributed to significant photoinduced electron transfer, resulting in nonradiativ
166 photoactivated living polymerization, named photoinduced electron transfer-reversible addition-fragm
168 e (ZnTPP)) were able to selectively activate photoinduced electron transfer-reversible addition-fragm
170 duction to the principle of fluorescent PET (photoinduced electron transfer) sensors and switches, th
172 (tau = 41 ps), whose excited state decays by photoinduced electron transfer (tau = 830 ps) to yield B
175 ely oxidize guanine were used to investigate photoinduced electron transfer through the DNA pi-stack
177 ion implicate a photoredox pathway involving photoinduced electron transfer to generate a key radical
178 ation of the porphyrin moiety is followed by photoinduced electron transfer to give a DHP-P(*)(+)-C(6
182 [Fe(II)cyt b562] folding can be triggered by photoinduced electron transfer to unfolded Fe(III)cyt b5
184 a unified design, based on the principle of photoinduced electron transfer, to access a panel of hig
185 osition 2, which are generated via oxidative photoinduced electron transfer, undergo anomalous fragme
186 clobutane pyrimidine dimers in DNA or RNA by photoinduced electron transfer using longer wavelength U
188 interactions between Pc and BQ, and exhibits photoinduced electron transfer with a lifetime of 40 ps
189 e porphyrin moiety of DHI-P-C(60) results in photoinduced electron transfer with a time constant of 2
190 hyrin gives DTEo-(1)P-C(60), which undergoes photoinduced electron transfer with a time constant of 2
191 f the porphyrin of BT-P-C(60) is followed by photoinduced electron transfer with a time constant of 5
192 zed" excited state of the complex reacts via photoinduced electron transfer with a variety of viologe
193 ellandrene and 4-methoxystyrene catalyzed by photoinduced electron transfer with tris(4-methoxyphenyl
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