ライフサイエンスコーパス: BODIPY

1 (PAH) luminophores and boron dipyrromethene (BODIPY).

2 ith the fluorescent dyes Alexa-Fluor 488 and Bodipy.

3 of a completely unsymmetrical trisubstituted BODIPY.

4 hearts were examined for presence of NPs and BODIPY.

5 ttached to the aryl at the meso positions of BODIPY.

6 t impact on J-aggregates and fluorescence of BODIPYs.

7 -S) cross-coupling reaction of the Biellmann BODIPYs (1a,b) and aryl- and heteroarylboronic acids in

8 bstituted di-, tri-, tetra-, and pentachloro-BODIPYs 2-5 were prepared.

9 The crystal structure of azaBODIPY-(BODIPY)2 triad revealed that the two BODIPY units were i

10 linked azaBODIPY-BODIPY dyads and azaBODIPY-(BODIPY)2 triads.

11 The BODIPY 2a exhibits strong D-A interaction with poor fluo

12 The tetraphenylethylene (TPE) substituted BODIPY 2a, and 2,3,3-triphenylacrylonitrile (TPAN) subst

13 igher fluorescence quantum yield compared to BODIPY 2a.

14 The single crystal structures of BODIPYs 2a and 2b reflect the planar orientation of meso

15 The photonic properties of BODIPYs 2a-2c were compared with 4-ethynylbenzonitrile s

16 The BODIPYs 2b and 2c show red-shifted absorption and emissi

17 ,3-triphenylacrylonitrile (TPAN) substituted BODIPYs 2b and 2c were designed and synthesized by the P

18 pared with 4-ethynylbenzonitrile substituted BODIPY 3 and phenylacetylene substituted BODIPY 4.

19 various analytes revealed that the azido-aza-BODIPY 3a selectively interacts with hydrogen sulfide (H

20 ted BODIPY 3 and phenylacetylene substituted BODIPY 4.

21 ation of an unprecedented 8-heteroaryl-fused BODIPY 4.

22 interactions, meso-(4-pyridinyl)-substituted BODIPY (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) dyes

23 Fmoc-Trp(C2-BODIPY)-OH contains a BODIPY (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) fluo

24 The [a]phenanthrene-fused BODIPYs 4a-c were characterized by NMR spectroscopy, HRM

25 In addition, BODIPYs 4b and 4c exhibit no toxicity in the light or da

26 tivation, staining intracellular lipids with BODIPY(505/515), and FACS-based isolation of top 0.5% li

27 ads based on the ratiometric fluorescent dye BODIPY 581/591.

28 The BODIPY 630/650 conjugate 28 (MRS4162) exhibited EC50 val

29 cal microscopy using radical-sensitive probe BODIPY(665/676).

30 BODIPY 7 bearing thienyl groups on the 2 and 6 positions

31 o-glycolic acid) (PLGA) NPs were loaded with BODIPY, a fluorophore, and percutaneously administered i

32 ensitizers derived from thieno-pyrrole-fused BODIPY (abbreviated as SBDPiR) and fullerene, C60 have b

33 le light where the two dye molecules (Ru and Bodipy) absorb with equal probability leads to the coope

34 l transformation shifts bathochromically the BODIPY absorption and permits the selective excitation o

35 lectrophiles, we have designed a fluorogenic BODIPY-acrolein probe, AcroB, that undergoes a >350-fold

36 s of BODIPY-ATP resulted in the formation of BODIPY-adenosine and phosphate ions.

37 The fluorescence of the generated BODIPY-adenosine was insensitive to the change in the co

38 donor-acceptor (D-A) interaction makes these BODIPYs AIE inactive.

39 IYIY-I2-BODIPY alone and in combination with PDT modulates the i

40 We have developed a fluorogenic Trp-BODIPY amino acid with a spacer-free C-C linkage between

41 in the literature that describes the use of BODIPY analogs for detecting alkaline phosphatase (ALP)

42 toxin (Ts1)-Bodipy, KIIIA-Bodipy, and GIIIA-Bodipy analogs.

43 Fluorescent boron dipyrromethene (BODIPY) analogs are often used as sensors for detecting

44 n the L-S reaction to give the corresponding BODIPY analogues in short reaction times and also with g

45 e photophysical properties of pyridine-based BODIPY analogues, dipyridylmethene dyes.

46 arge-separated state composed of an oxidized Bodipy and a reduced Ru.

47 their corresponding BF2-chelated derivatives BODIPY and aza-BODIPY, respectively, are well known for

48 udies indicated a weak interaction among the BODIPY and azaBODIPY moieties and the moieties retain th

49 mphiphilic arrays containing PEG-substituted BODIPY and chlorins or bacteriochlorins were prepared an

50 gid structural conformation of the precursor BODIPY and the high reactivity of its 1,7-bromo groups.

51 are the sum of the individual chromophores (Bodipy and the PtN2S2 moieties), indicating little elect

52 l-2,6-diethyl-4-bora-3a,4a-diaza-s-indacene (Bodipy) and a Ru(II)(bipyridine)3 (Ru) derivative-which

53 ed fluorophore such as boron-dipyrromethene (BODIPY) and BF2-smaragdyrin under mild Pd(0) coupling co

54 t, IYIY-diiodo-boron-dipyrromethene (IYIY-I2-BODIPY) and its scrambled counterpart YIYI-I2-BODIPY hav

55 g triphenylphosphonium, borondipyrromethene (BODIPY), and triazacryptand (TAC).

56 regioselectively from 2,3,5,6,8-pentachloro-BODIPY, and characterized by NMR spectroscopy, HRMS, and

57 ors: beta-scorpion toxin (Ts1)-Bodipy, KIIIA-Bodipy, and GIIIA-Bodipy analogs.

58 pression analysis, dihydroethidium staining, BODIPY, and quantification of intracellular triglyceride

59 observed for all the aforementioned PAHs and BODIPY, and the rubrene and BODIPY emulsion systems show

60 complexes, A3-, A2B- and AB2-type corroles, BODIPYs, and their dipyrrane precursors was studied util

61 d antioxidant (chromanol) and prooxidant (Br-BODIPY) antagonistic chemical activities of the two-segm

62 Heavy atom-free BODIPY-anthracene dyads (BADs) generate locally excited

63 fluorescence properties of these conjugated BODIPYs are also described.

64 Cryptopyrrole-derived oligo-BODIPYs are characterized by a tight intramolecular arra

65 Structure features of new BODIPYs are discussed within the context of 14 new X-ray

66 t the potential use of [a]phenanthrene-fused BODIPYs as NIR bioimaging probes.

67 For both series of arrays, excitation of BODIPY at 500 nm results in efficient energy transfer to

68 e fluorescence of chlorin upon excitation of BODIPY at approximately 500 nm.

69 ordination between the triphosphate group of BODIPY-ATP and Fe(3+)/Fe(2+) on the NP surface.

70 he Fe(III)-induced fluorescence quenching of BODIPY-ATP can be paired with its ALP-mediated dephospho

71 ound that pyrophosphate and ATP compete with BODIPY-ATP for binding to Fe3O4 NPs.

72 BODIPY-ATP molecules attached to the surface of Fe3O4 NP

73 The ALP-catalyzed hydrolysis of BODIPY-ATP resulted in the formation of BODIPY-adenosine

74 of BODIPY-conjugated adenosine triphosphate (BODIPY-ATP) was quenched by Fe(III) ions through photoin

75 Dyads with BODIPY attached at the 10-position of chlorin exhibit a

76 fluorescence quantum yields and lifetimes of BODIPY attached to the two S16 homologs decreased gradua

77 of the fluorescence quenching efficiency of BODIPY-AuNPs in the presence of thiols can achieve a lar

78 Combining a squaraine (S) and a BODIPY (B) chromophore in a heterodimer (SB) and two het

79 vatives, with absorption between 500-700 nm, BODIPY-bacteriochlorin arrays should allow for construct

80 Luminescence properties of the BODIPY-based chemodosimetric reagent make it an ideal ca

81 physicochemical properties of a new class of BODIPY-based donor-acceptor pi-conjugated polymers are p

82 oieties conjugated to nonpolar coumarin- and BODIPY-based fluorophores.

83 , we report synthesis and application of new BODIPY-based hydrophobic sensors (HPsensors) that are st

84 We report a BODIPY-based luminescence ON reagent for detection of HN

85 nt charge-transport improvement (>10000x) in BODIPY-based polymeric semiconductors, demonstrating its

86 We have designed a low fluorescent azido-BODIPY-based probe AzBOCEt (Az10) that undergoes copper(

87 We have designed a BODIPY-based probe called (S)-Sulfox-1, which is equippe

88 A series of push-pull BODIPYs bearing multiple electron-donating and electron-

89 c substitution and led to the isolation of F-BODIPYs bearing terminal bromovinyl and enol substituent

90 IYIY-I2-BODIPY binds TrkC similar to neurotrophin-3 (NT-3), and

91 ctron donating group at the meso position of BODIPY blue shifts the absorption and emission with decr

92 th alcohols and phenols can be tagged with a BODIPY (borondipyrromethene) moiety to yield highly fluo

93 aterials bear close structural similarity to BODIPYs but differ significantly in electronic configura

94 me imaging microscopy of the molecular rotor BODIPY C10 in the membranes of live Escherichia coli bac

95 ppressive conventional chemotherapy, IYIY-I2-BODIPY can act as an immune-stimulatory chemotherapeutic

96 72 nm, Phi(F) = 19% for 7) from those of the BODIPY-carboxaldehydes 2b (lambda(abs) = 643 nm and lamb

97 reaction is an interesting synthetic tool in BODIPY chemistry, mainly because it allows a valuable re

98 t here the synthesis and characterization of BODIPY-chlorin arrays containing a chlorin subunit, with

99 t the difference in lateral diffusion of the BODIPY-cholesterol probes was not caused by anomalous su

100 ce of thiols, meso-(4-pyridinyl)-substituted BODIPY chromophore were displaced and released from the

101 rfaces and thus restored the fluorescence of BODIPY chromophore.

102 uoroionophore based on a bright red-emitting BODIPY chromophore.

103 ive compounds combine a borondipyrromethene (BODIPY) chromophore and a photocleavable oxazine within

104 carbon monoxide-releasing molecules based on BODIPY chromophores (COR-BDPs) activatable by visible-to

105 ylbutadiene-conjugated or styrene-conjugated BODIPY chromophores (PBD-BODIPY or STY-BODIPY, respectiv

106 s were instead observed between at least two BODIPY chromophores along the edges of the cages, arisin

107 ultrafast dynamics of electronically excited BODIPY chromophores could lead to further advances in th

108 e report a set of Fe(II)4L6 cages containing BODIPY chromophores having tuneable photosensitizing pro

109 ompare the ultrafast dynamics of halogenated BODIPY chromophores through applying two-dimensional ele

110 able regioselective postfunctionalization of BODIPY chromophores with different functional groups.

111 ompare the results of structurally different BODIPY chromophores.

112 es, as well as mixed cages that contain both BODIPY chromophores.

113 ctronic states of the structurally different BODIPY chromophores.

114 Boron-dipyrromethene (BODIPY) chromophores have a wide range of applications,

115 ht-activated release of bioactive compounds (BODIPY, colchicine, paclitaxel, and methotrexate) from m

116 res, and photophysical parameters of all new BODIPY compounds are reported and discussed.

117 BODIPY-maleimide provided a dye-labeled pOEG-BODIPY conjugate with a lower critical solution temperat

118 is study discovered that the fluorescence of BODIPY-conjugated adenosine triphosphate (BODIPY-ATP) wa

119 The coumarin- and BODIPY-conjugated amine probes described here undergo 38

120 In summary, our Tb-Bodipy conjugates could help us to reveal the molecular

121 A novel BODIPY-containing organic small molecule is synthesized

122 DIPY (weak response) at 10 mg/kg, but not I2-BODIPY control, increased the levels of IL-2, IL-4, IL-6

123 anar orientation of meso substituent and the BODIPY core, which leads to close pi-pi stacking.

124 onic communication between the 8-OPh and the BODIPY core.

125 l planar N atoms which are coplanar with the BODIPY core; 4 exhibits a very significant distortion th

126 based on a ring-fused boron-dipyrromethene (BODIPY) core that is conjugated to a polyglycerol dendri

127 Relying on the boron-dipyrromethene (BODIPY) core, all the probes as well as selected referen

128 aration of the labeled antimicrobial peptide BODIPY-cPAF26 by solid-phase synthesis (6-7 d) and its s

129 an example, we include a procedure for using BODIPY-cPAF26 for wash-free imaging of fungal pathogens,

130 3.Et2O in moist CH2Cl2 to regenerate the BF2-BODIPYs (demasking).

131 The aza-BODIPY derivative 3b, on the other hand, exhibited selec

132 In contrast, the dimethylamino-aza-BODIPY derivative, 3c, showed negligible affinity for th

133 ready precursors of ortho-substituted 8-aryl BODIPY derivatives by reaction with borontrifluoride eth

134 t synthesis of a new class of conjugated aza-BODIPY derivatives from readily available precursors has

135 absorbing and emitting bacteriochlorin, and BODIPY derivatives with different absorption bands in th

136 we synthesized three novel NIR absorbing aza-BODIPY derivatives, 3a-3c, and have systematically tuned

137 Given the availability of diverse BODIPY derivatives, with absorption between 500-700 nm,

138 Boron dipyrromethene (BODIPY) derivatives have found widespread utility as chr

139 We also found that N-BODIPY detects aggregation of peroxisomes during final s

140 A and pore-network development and increased BODIPY diffusion coefficient, resulting in faster releas

141 he masking strategy was used to synthesize a BODIPY dimer by McMurry coupling of a formyl Et2B-BODIPY

142 New dyads consisting of a strongly absorbing Bodipy (dipyrromethene-BF2) dye and a platinum diimine d

143 ants exhibited a decrease in the average Trp-BODIPY distance at up to 100 mg/mL dextran 20, whereas t

144 ermo mutants did not show any changes in Trp-BODIPY distances upon increase of dextran 20 concentrati

145 he different regions of the heart influenced BODIPY distribution, with fluorophore penetrating more r

146 3.Et2O to obtain covalently linked azaBODIPY-BODIPY dyads and azaBODIPY-(BODIPY)2 triads.

147 We conjugated Tb with a green-emitting Bodipy dye attached by alternative linkers of different

148 In these dyads, the Bodipy dye is bonded directly to the benzenedithiolate l

149 tion range can be tuned by the choice of aza-BODIPY dye or/and the hydrogel matrix.

150 metric photoacoustic imaging by using an aza-BODIPY dye scaffold exhibiting two spectrally resolved N

151 applies to a maleimide derivative carrying a BODIPY dye which was chosen for its fluorescence to be o

152 t example of the use of a molecular rotor, a BODIPY dye, to quantitatively visualize the viscosity of

153 irms this fluorescence to originate from the BODIPY dye.

154 ic interaction between the squaraine and the BODIPY dye.

155 study on donor/acceptor borondipyrromethene (BODIPY) dye-labeled cavitands present in the vase and ki

156 ts of a Br-substituted boron-dipyrromethene (BODIPY) dye.

157 The BODIPY dyes bearing alkoxy or nonfunctionalized phenoxy

158 This review summarizes the attributes of BODIPY dyes for PDT, and in some related areas.

159 ith the outstanding absorption properties of BODIPY dyes lead to photocages with uncaging cross secti

160 tecting groups derived from meso-substituted BODIPY dyes release acetic acid with green wavelengths >

161 -PMHC and related bromo and iodo-substituted BODIPY dyes show that the trap segment provides a total

162 ugh the judicious functionalization, the aza-BODIPY dyes thus synthesized can be utilized for the sen

163 Distance distributions between the BODIPY dyes were established by comparing time-resolved

164 Eleven formyl-containing BODIPY dyes were prepared by means of either the Liebesk

165 sorption and fluorescence spectra of the aza-BODIPY dyes with the change in substitution from azido (

166 lified by the preparation of a series of new BODIPY dyes with unprecedented substitution patterns all

167 lectron deficient backbones, the BF2 unit of BODIPY dyes, and AlF or GaF3 units coordinated to multid

168 asserini reaction to give highly substituted BODIPY dyes.

169 Fluorescent dithienyl-borondipyrromethene (BODIPY) dyes formylated in the beta'-position (2b, 2c) h

170 nstructed from extended borondipyrromethene (BODIPY) dyes, diketopyrrolopyrrole (DPP) dyes, and elect

171 helated tetraarylazadipyrromethene dyes (aza-BODIPYs) dyes physically entrapped in polyurethane hydro

172 ntioned PAHs and BODIPY, and the rubrene and BODIPY emulsion systems showed adequate light to record

173 Only IYIY-I2-BODIPY enhanced the IFN-gamma(+) and IL-17(+) T-lymphocy

174 ve emission from bacteriochlorin moiety upon BODIPY excitation.

175 The BODIPYs exhibited low dark toxicity and phototoxicity to

176 ies, including fluorescein, Alexa Fluor 488, BODIPY FL, and rhodamine 6G.

177 ysis kinetics and were active in hydrolysing BODIPY-FL casein to varying extents at postmortem aging

178 BODIPY-FL-pentanoic-acid staining revealed higher short

179 reduction to the hydroquinone form, B-VKQH2, BODIPY fluorescence is restored, with emission quantum y

180 n thinner sheet packages which still exhibit BODIPY fluorescence right at the rim of these packages.

181 ting principles allow the photoactivation of BODIPY fluorescence with large brightness and infinite c

182 py)(H2O)3][O2CCH3] (1), which incorporates a bodipy fluorescent tag, was prepared and studied by conf

183 The incorporation of our unique BODIPY fluorogen in biologically relevant peptides will

184 a spacer-free C-C linkage between Trp and a BODIPY fluorogen, which shows remarkable fluorescence en

185 by confocal fluorescence microscopy using a Bodipy fluorogenic substrate.

186 curring lipid soluble antioxidant, while the BODIPY fluorophore and TPP ensure partitioning within th

187 apabilities of this system introduction of a BODIPY fluorophore as a secondary functionality was perf

188 o series of activity-based probes carrying a BODIPY fluorophore for alpha-l-fucosidase.

189 an alpha-tocopherol-like chromanol moiety, a BODIPY fluorophore, and a triphenylphosphonium cation (T

190 etween the photochrome and a co-encapsulated BODIPY fluorophore.

191 ne redox center), to a boron-dipyrromethene (BODIPY) fluorophore (a lipophilic reporter segment).

192 oquinone, coupled to a boron-dipyrromethene (BODIPY) fluorophore segment that both imparts lipophilic

193 es can guide future design of functionalized BODIPYs for various applications, including bioimaging a

194 g cleaves irreversibly to bring the adjacent BODIPY fragment in conjugation with an indole heterocycl

195 A series of seven BODIPYs functionalized with ortho-carborane groups at th

196 ar weight (Mw), water uptake, mass loss, and BODIPY (green-fluorescent dye) diffusion coefficient in

197 The BODIPY group was attached at three specific positions in

198 ODIPY) and its scrambled counterpart YIYI-I2-BODIPY have been prepared.

199 lar cycloaddition yielding the first corrole-BODIPY heterodimer involving the pentafluorosulfanyl gro

200 that the 2,2'-bipyridine spacer of each bpy-BODIPY homologue does not facilitate efficient electroni

201 BODIPY-hydroporphyrin energy transfer arrays allow for d

202 he immunological impacts mediated by IYIY-I2-BODIPY in pre- and post-PDT conditions.

203 led distinct tyrosine quenching behaviors of BODIPY in the three variants, suggesting a dynamic local

204 action was employed to synthesize conjugated BODIPYs in high yields by treating formylated BODIPYs wi

205 c purification on silica afforded conjugated BODIPYs in ~65-90% yields.

206 efficiently, and we prepared 12 substituted BODIPYs including cholesterol-substituted BODIPYs to dem

207 monstrated on the basis of selected starting BODIPYs, including polyhalogenated and/or asymmetrical s

208 T effects (drug-light interval 1 h), IYIY-I2-BODIPY induced stronger responses.

209 cedures (e.g., asymmetrically functionalized BODIPYs involving halogenated positions) can now be made

210 Overall, dyads where BODIPY is attached at the 10-position of chlorin exhibit

211 ositions of chlorin, and a second type where BODIPY is attached at the 10-position of chlorin through

212 ontrast to this, some of the arrays in which BODIPY is attached at the 3- or at both 3,13-positons of

213 The pentachloro-BODIPY is shown to undergo regioselective Pd(0)-catalyze

214 this work, the energy donor moiety (distyryl-BODIPY) is connected to a photosensitizer (i.e., diiodo-

215 4,4-difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) is reported.

216 ized as acceptors: beta-scorpion toxin (Ts1)-Bodipy, KIIIA-Bodipy, and GIIIA-Bodipy analogs.

217 stances between an intrinsic Trp residue and BODIPY-labeled S16Meso depend on the level of the crowdi

218 Three different Bodipy-labeled, Nav1.4-targeting toxins were synthesized

219 nt Arabidopsis mutant atg5 correlated with N-BODIPY labeling.

220 bioconjugates brought clear evidence that Tb-Bodipy localized in the endoplasmic reticulum (ER) of va

221 All BODIPYs localized mainly within the cell ER.

222 frared (NIR) thanks to delocalisation of the BODIPY low-lying lowest unoccupied molecular orbital (LU

223 new emissive species is formed from the bpy-BODIPY luminophores during the annihilation process.

224 End-group modification with fluorescent BODIPY-maleimide provided a dye-labeled pOEG-BODIPY conj

225 e route for transforming BF2-BODIPYs to Et2B-BODIPYs (masking) was developed using Et2AlCl.

226 Two types of arrays were examined: one where BODIPY moieties are attached through a phenylacetylene l

227 ep-red (641-685 nm) emission, and one or two BODIPY moieties, absorbing at 504 nm.

228 containing one or the other of two distinct BODIPY moieties, as well as mixed cages that contain bot

229 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) moieties, which we symmetrically conjugate with

230 to various chain lengths of ethylene-bridged BODIPY motifs was discovered.

231 ies higher than that in the reference dyads (Bodipy-NDI and TAPD-Ru), leading to the energy efficienc

232 tude compared to that in the reference dyads Bodipy-NDI and TAPD-Ru, as it passes from about 3 ns in

233 The tetrad Bodipy-NDI-TAPD-Ru is composed of two different dyes-4,4

234 is of the fluorogenic amino acid Fmoc-Trp(C2-BODIPY)-OH (3-4 d), the preparation of the labeled antim

235 rp)-based fluorogenic amino acid Fmoc-Trp(C2-BODIPY)-OH and its incorporation into peptides for live-

236 Fmoc-Trp(C2-BODIPY)-OH contains a BODIPY (4,4-difluoro-4-bora-3a,4a-

237 styrene-conjugated BODIPY chromophores (PBD-BODIPY or STY-BODIPY, respectively) as signal carriers t

238 the environmentally insensitive fluorophore BODIPY or the pH-sensitive dye pHrodo red.

239 Treatment of 3,5-diformyl BODIPYs or alpha-formyl 3-pyrrolyl BODIPY with different

240 ditive, for example, a 2,6-diiodo-B-dimethyl BODIPY photocage features quantum yields of 28% for the

241 and photochemical reactivity of meso-methyl BODIPY photoremovable protecting groups was accomplished

242 on that breaks the planarity of the extended BODIPY pi system due to the steric impact of the two eth

243 attempt to develop photostable and efficient BODIPY (PM) dyes for use in liquid dye lasers, three new

244 d AzG-1, a cyclooctyne- and azide-containing BODIPY probe, respectively, which specifically label int

245 4'-di fl uoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) probes is systematically investigated to demonst

246 BODIPY proved to have a long-term presence within the he

247 th a variety of azido derivatives, including Bodipy, pyrene and ferrocene, was carried out first.

248 the origin of this decrease, we studied the BODIPY quantum yield in three protein variants in the pr

249 imple (small, nonaggregated, nonpolymeric) O-BODIPYs (R)-1 and (S)-1 by irradiation with visible ligh

250 on withdrawing group at the meso position of BODIPY red shifts the absorption and emission with enhan

251 f the final charge-separated state (oxidized Bodipy/reduced Ru) in the tetrad lies higher than that i

252 gated BODIPY chromophores (PBD-BODIPY or STY-BODIPY, respectively) as signal carriers that co-autoxid

253 ding BF2-chelated derivatives BODIPY and aza-BODIPY, respectively, are well known for fluorescence-ba

254 In vitro, fluorescent CLR1404-BODIPY showed significant selective uptake in a variety

255 The BODIPYs showed higher permeabilities than lucifer yellow

256 In this way, the BODIPY-squaraine conjugates combine the best properties

257 is is caused by intensity borrowing from the BODIPY states, which increases the squared transition mo

258 We demonstrated that IYIY-I2-BODIPY (strong response) and YIYI-I2-BODIPY (weak respon

259 In a tandem solar cell comprising a NIR BODIPY subcell and a matching "green" absorber subcell,

260 character exhibited by the bis(aminophenyl)-BODIPY subcomponents disappeared.

261 eric demand of the alkyl substituents in the BODIPY subunit defines the site of (1)O2 addition.

262 atment with BF3.Et2O gives a 3,5,8-trichloro-BODIPY that readily undergoes regioselective Stille coup

263 ed large functional groups including biotin, BODIPY, thiazole orange, and Cy7 through a polyethylene

264 These effects on the BODIPY-TMR-CGP dissociation rate were markedly enhanced

265 The dissociation rate of 3 nM BODIPY-TMR-CGP was 0.09 +/- 0.01 min(-1) in the absence

266 methane-tetramethylrhodamine-(+/-)CGP 12177 (BODIPY-TMR-CGP)] at the human beta1-adrenoceptor express

267 an efficient (>/=0.80) energy transfer from BODIPY to the chlorin moiety in both toluene and DMF and

268 ed BODIPYs including cholesterol-substituted BODIPYs to demonstrate the versatility of the reaction.

269 nd chemoselective route for transforming BF2-BODIPYs to Et2B-BODIPYs (masking) was developed using Et

270 to a photosensitizer (i.e., diiodo-distyryl-BODIPY) to form a dyad molecule (RET-BDP).

271 f a lipophilic fluorogenic antioxidant (Mito-Bodipy-TOH) that targets the inner mitochondrial lipid m

272 Moreover, photoirradiated IYIY-I2-BODIPY treated mice had high levels of effector T-cells

273 optive transfer of immune cells from IYIY-I2-BODIPY-treated survivor mice that were photoirradiated g

274 the fluorescent-dye conjugate, [S14R, W50Pra(Bodipy)]Ts1, we confirmed its binding to Nav1.4 through

275 ional groups was approached with a dual-mode BODIPY-type fluorescence label, which allows quantificat

276 The application of a multimode BODIPY-type fluorescence, photometry, and X-ray photoele

277 supported an efficient energy transfer from BODIPY unit(s) to azaBODIPY unit in dyads and triads.

278 BODIPY-(BODIPY)2 triad revealed that the two BODIPY units were in perpendicular orientation with azaB

279 stepwise methodology for polychlorination of BODIPY using trichloroisocyanuric acid (TCCA) in acetic

280 use single-Q-loop mutants are functional for Bodipy-verapamil transport.

281 tive antibody (UIC2) and a fluorescent drug (Bodipy-verapamil), respectively.

282 as further reacted with an azido-substituted BODIPY via the copper(I)-catalyzed 1,3-dipolar cycloaddi

283 very useful for synthesizing functionalized BODIPYs via nucleophilic and reductive reactions.

284 s were mostly confined to epicardial layers, BODIPY was capable of penetrating into the myocardium, r

285 Absorption band of BODIPY was tuned by installation of 0, 1, or 2 styryl su

286 ctroscopic and electrochemical properties of BODIPYs was investigated.

287 chelated tetraarylazadipyrromethene dye (aza-BODIPY) was incorporated into the polyvinylpyrrolidone s

288 IYIY-I2-BODIPY (strong response) and YIYI-I2-BODIPY (weak response) at 10 mg/kg, but not I2-BODIPY co

289 diphenylanthracene, pyrene, or perylene) and BODIPY were trapped in a toluene and tri-n-propylamine m

290 w fluorescence quantum yields, the push-pull BODIPYS were effective for cell imaging, readily accumul

291 All BODIPYs were nontoxic in the dark (IC50 > 200 muM) and s

292 Several examples of unsymmetrical BODIPYs were synthesized and characterized using this me

293 xisome abundance using the small probe Nitro-BODIPY, which in vivo fluoresces selectively inside pero

294 Y dimer by McMurry coupling of a formyl Et2B-BODIPY, while a new BODIPY with an asymmetrically substi

295 oupling of a formyl Et2B-BODIPY, while a new BODIPY with an asymmetrically substituted B-center was s

296 -diformyl BODIPYs or alpha-formyl 3-pyrrolyl BODIPY with different alkyl/aryl ylides in CH2Cl2 at roo

297 Spiro-BODIPYs with a diaryl chelate unit have been found to fo

298 ODIPYs in high yields by treating formylated BODIPYs with alkyl/aryl ylides under simple room tempera

299 The first series of arrays contains BODIPYs with PEG substituents attached to the boron, whe

300 Three furan fused boron dipyrromethenes (BODIPYs) with a CF3 group on the meso-carbon are synthes