ライフサイエンスコーパス: absorption band

1 and 950cm(-1) (glucose, fructose and sucrose absorption bands).

2 optical intervalence charge-transfer (IVCT) absorption band.

3 y tuning the pump laser into the gain medium absorption band.

4 e--after optical excitation tuned to the CDW absorption band.

5 t light scatters around the nanogold plasmon absorption band.

6 y 5-nm red shift of the long wavelength Q(y) absorption band.

7 the strength of the lowest-energy two-photon absorption band.

8 approximately 30 nm blue shift of the dimer absorption band.

9 escence from the blue to the red side of the absorption band.

10 residues, as reflected by changes in the UV absorption band.

11 ee ligand absorption and increase of complex absorption band.

12 hromic shift of its lowest energy electronic absorption band.

13 lexes producing new red-shifted emission and absorption bands.

14 ong electronic transitions of photosynthetic absorption bands.

15 essively red-shifted primary charge-transfer absorption bands.

16 nent spectra with overlapped or superimposed absorption bands.

17 dders revealed both polaron and intervalence absorption bands.

18 ole in determining the line shape of such CT absorption bands.

19 -unsaturated ketones are split into distinct absorption bands.

20 s due to the presence of intrinsic vibration absorption bands.

21 liquid solutions for different emission and absorption bands.

22 ing agents with multiple and broadly tunable absorption bands.

23 utions of the IL used in this study show two absorption bands.

24 to the absolute positions of the water vapor absorption bands.

25 ndow corresponding to the protein Amide I/II absorption bands.

26 g. by means of studying characteristic water absorption bands.

27 es weaker than those of the strongest mid-IR absorption bands.

28 a separation of the E and Z isomers' n-->pi* absorption bands.

29 o a second excited state with two CN-stretch absorption bands.

30 iochlorophylls), with a strong near-infrared absorption band (707-751 nm).

31 roposed that in S65T/H148D, the red shift of absorption band A and the ultrafast appearance of green

32 that hypochromism induced in the tryptophan absorption band, a ground-state effect, is a significant

33 and the variant S65T/H148D each exhibit two absorption bands, A and B, which are associated with the

34 ssignment of the observed MCD and electronic absorption bands, a detailed understanding of the metal-

35 The lowest Q(y) state in absorption band (A1) is characterized by an electron-pho

36 phan oxidation products exhibited a distinct absorption band above 280 nm shifted to the longer wavel

37 proteins give rise to nine characteristic IR absorption bands (amides A, B and I-VII).

38 They are also characterized by a wide absorption band and a narrow emission band, which makes

39 show this species to have a distinct visible absorption band and a transition moment that we suggest

40 rized by a 1017 nm bacteriochlorophyll anion absorption band and decays by charge recombination with

41 ystine was quantitated using its 1296 cm(-1) absorption band and levels matched with parallel measure

42 Spectral overlap between the azobenzene absorption band and plasmonic resonances of silver nanow

43 engths corresponding to the hemoglobin Soret absorption band and to the absorption bands of the dyes

44 avelengths within both the H and J aggregate absorption bands and are imaged on the surface of silica

45 rmined from the intervalence charge-transfer absorption bands and from electronic structure calculati

46 osition produces a bathochromic shift of all absorption bands and makes alpha and beta bands equal as

47 s have enhanced and bathochromically shifted absorption bands and much better solubility in organic s

48 the absorption edge, appearance of a new IR absorption band, and Auger quenching of the excitonic ph

49 idation potential, bathochromic shift of the absorption band, and minimization of the emission quantu

50 lly result in hypsochromic shifts in various absorption bands, and (4) the bulk of the red-shift comm

51 gap between their first and second excitonic absorption bands, and this narrowing effect is size-depe

52 )18 clusters exhibit multiple molecular-like absorption bands, and we find the results are in good co

53 Intervalence absorption bands appearing in the diagnostic near-IR reg

54 For one of the anionic guests, a visible absorption band appears upon host-guest formation with t

55 de aerosol substrates exhibits a red-shifted absorption band ( approximately 450-650 nm) consistent w

56 profiles in resonance with the lowest energy absorption band are measured.

57 to all of the excitation profiles and to the absorption band are obtained using one set of excited-st

58 ET barriers evaluated from the intervalence absorption bands are also quantitatively verified by the

59 The shapes of the charge-transfer absorption bands are analyzed in the framework of a dyna

60 quaraine (SQ) donor molecules with different absorption bands are blended together for better coverag

61 nd the direction of electron oscillations in absorption bands are discussed.

62 erization, and the relative positions of all absorption bands are found to be in agreement with the e

63 2), Broad, "dimer" absorption bands are observed for both P700(+) and P740(

64 n the colloids are in proximity, the plasmon absorption bands are often perturbed.

65 ults for Mn-depleted PS II, multiple near-IR absorption bands are resolved in the light-minus-dark di

66 , and it has long been a mystery why Vesta's absorption bands are so strong.

67 inating ruthenium to the thiophenes is a new absorption band around 470 nm.

68 ecifically, it exhibits a blue-shifted broad absorption band around 500 nm and a rR spectrum with a n

69 The UV-vis spectrum of 1 shows a broad absorption band around 550 nm that is assigned to a char

70 Complex 1 is characterized by a broad absorption band around 600 nm that is assigned to a char

71 tions of the location of seven near-infrared absorption bands as functions of temperature 5-50 degree

72 nd UV-vis detection allows observation of an absorption band assigned to singlet 2-oxocyclohexa-3,5-d

73 the dimer radical cation was replaced by an absorption band assigned to the (alpha-thio)benzyl catio

74 nges and the significance of charge-transfer absorption bands associated with the reduction of FAD by

75 sor of this reactive site with an associated absorption band at 29,000 cm(-1).

76 AMAM dendrimer results in a strong, distinct absorption band at 300 nm, making UV-vis spectrophotomet

77 rified phosphopyridoxyl peptide exhibited an absorption band at 325 nm, and its identity was further

78 In the presence of 4-hydroxypyridine, a new absorption band at 338 nm, assigned to the alpha-aminoac

79 were accompanied by the appearance of a new absorption band at 376 nm in the UV-vis spectrum consist

80 ded Ag quantum dots show a plasmon resonance absorption band at 438 nm.

81 broad metal-to-ligand charge transfer (MLCT) absorption band at 450 nm with epsilon = 1.7 x 10(4) M(-

82 panied by the concomitant loss of the flavin absorption band at 458 nm.

83 recombinant KDO8PS, as isolated, displays an absorption band at 505 nm and contains approximately 0.4

84 o form brown carbon (BrC) with a distinctive absorption band at 505 nm.

85 icity in the absence of substrate and a weak absorption band at 508 nm.

86 f AMTr-AuNPs was changed into purple and the absorption band at 520 nm was decreased.

87 With substrate present, however, an intense absorption band at 555 nm (epsilon = 150-175) with a neg

88 ile the corresponding dication afforded this absorption band at 629 nm.

89 ical interactions, which give rise to an NIR absorption band at 900 nm, tend to play a crucial role i

90 In contrast, the energy of the absorption band at about 295 nm, designated as pi(CS) --

91 ants, an additional chromophore band with an absorption band at about 480 nm was observed, which was

92 decrease in the magnitude of the UV-visible absorption band at approximately 400 nm that we attribut

93 perties with compounds showing a high-energy absorption band at ca. 270-290 nm and a low-energy band

94 window corresponding to the protein Amide A absorption band at dilution by a factor of 900 (0.034% w

95 tions of 1 in THF-d8 possess a strong UV-vis absorption band at lambda(max) approximately 640 nm.

96 the aggregate of DD-PTCDI shows a pronounced absorption band at the longer wavelength, whereas the ab

97 ized tryptophan residue exhibited a distinct absorption band at the maximum absorbance wavelength 335

98 Two sharp absorption bands at 1418 cm(-1) and 3323 cm(-1) were att

99 ved IR (TRIR) spectroscopy as characteristic absorption bands at 1814, 2101, and 2038 cm-1, respectiv

100 tion of ciprofloxacin, PVD showed new UV-vis absorption bands at 252 and 321nm due to an internal cha

101 The Pb(II) complex reveals two prominent absorption bands at 350 nm (epsilon = 4000 M(-1) cm(-1))

102 sis is colorless, but turns green with broad absorption bands at 430 and 680 nm after reconstitution

103 imonene SOA, both of which produced BrC with absorption bands at 475 and 505 nm, respectively.

104 On FdTt unfolding at alkaline pH, new absorption bands at 520 nm and 610 nm appear transiently

105 au = 333 ns, kobs = 3.0 x 106 M-1s-1) having absorption bands at 570 and 620 nm in CH3CN.

106 nm from carotenoids as well as smaller Q(y) absorption bands at 672 and 812 nm from chlorophyll a an

107 ynthesized Ar4TNPs exhibit remarkably strong absorption bands at 710-720 nm (epsilon approximately 20

108 ure of at least two species characterized by absorption bands at approximately 607 nm (P607) and appr

109 tylimide ring, exhibits the most red-shifted absorption band (at lambda(max) = 746 nm), the lowest fl

110 NikD exhibits an unusual long wavelength absorption band attributed to a charge transfer complex

111 ds, including a unique low-energy electronic absorption band, attributed to an IVCT-type transition t

112 however, exhibits an unusual long-wavelength absorption band, attributed to charge-transfer interacti

113 We observe multiple absorption bands but no cross peaks in the 2D IR spectra

114 The polarons of F(3) and F(4) display sharp absorption bands, but for longer oligomers the bands bro

115 of excited states are characterized by a red absorption band (ca. 600 nm) assigned to Co 3d --> 3d or

116 as reflectivity and spectral position of the absorption band can be varied in situ within +/-0.5 V.

117 l results indicate that the bandwidth of the absorption bands can be controlled by changing the diele

118 y using mixtures of D(2)O and H(2)O, water's absorption bands can be made to be on-scale in transmiss

119 ngths beyond 800 nm, clearly outside the LWC absorption bands, can still induce photochemical charge

120 Following excitation of the high-energy absorption band centered at 398 nm and assigned to the n

121 n around 1510 cm(-1) and a visible transient absorption band centered at 760 nm.

122 arge-transfer complex with a long-wavelength absorption band centered at 780 nm.

123 e asteroid Vesta has prominent near-infrared absorption bands characteristic of a range of pyroxenes,

124 FTIR of the coatings showed absorption bands characteristic of phosphate groups, and

125 d a 2-fold slower decay of the excited-state absorption bands compared to the monomer M (tau4,foldame

126 nd MEH-PPV oligomers, the calculated intense absorption bands converge at the longest wavelengths for

127 intensity of the resulting particle plasmon absorption bands correlates well with the redox characte

128 which displayed no enzymatic activity and no absorption band corresponding to an internal PLP-aldamin

129 The CO adduct of T67R/S92D shows two CO absorption bands corresponding to the A(1) and A(3) subs

130 The subpicosecond transient absorption bands decay may reflect rapid charge separati

131 The presence of two CN-stretch absorption bands demonstrates that this secondary excite

132 n and had the same lifetime as the transient absorption band detected in the visible region, confirmi

133 However, the visible absorption band does not match that of the monomeric cat

134 ids are well known to display strong plasmon absorption bands due to electron oscillations induced by

135 at least one of the lower-energy electronic absorption bands (E(max) approximately 16300 cm(-1)) is

136 rgies below the band edge, whereas above the absorption band edge of hematite, the surface plasmon po

137 Large red shifts of the UV/vis absorption bands evidence efficient incorporation of the

138 Both absorption bands exhibit a modest negative solvatochromi

139 The SPR absorption band exhibits an exceptional behavior: As siz

140 ded pentafulvenes feature intense electronic absorption bands, extending over the entire visible spec

141 ure is increased from low temperature, a new absorption band for the unfolded protein grows in and th

142 Compared to the wild type, the Qy absorption bands for BChl c in the mutant cells were nar

143 Weak CT absorption bands for D-A complexes occur at photon energ

144 stematically examined, and characteristic IR absorption bands for the corresponding N-trifluoromethan

145 The observed UV-visible absorption bands for the Fe(3+)-nitrile intermediate spe

146 H complex is 200 microM with charge-transfer absorption bands for the KMO(RED).l-Kyn.NADP(+) complex

147 dent response of the diagnostic intervalence absorption bands for the quantitative evaluation of the

148 ectra of glycosylated proteins show distinct absorption bands for the sugar moiety, the protein amide

149 of the molecules' dipole moments and J-type absorption band formation in thin films.

150 aid in the assignment of the intense near-UV absorption bands found for the oxoiron(IV) complexes wit

151 tivates the enzyme and shifts the electronic absorption band from 420 to 325 nm.

152 ailed analysis because of the absence of the absorption bands from heme b(595).

153 during nanowire growth by comparing nu(Ge-H) absorption bands from operando measurements (i.e., durin

154 redox difference spectroscopy has identified absorption bands from the COOH group of E107.

155 Similar long-wavelength absorption bands have been observed for flavoproteins co

156 perimental results indicate that the amide I absorption band in D(2)O (i.e., amide I') attributable t

157 y the lack of a detectable 1-micrometer Fe2+ absorption band in high-spatial-resolution spectra of ma

158 ort here the observation of a giant-infrared-absorption band in reduced graphene oxide, arising from

159 (3)OC(6)H(4)CN(2)CH(3)) produced a transient absorption band in the 400-700 nm region.

160 the hypsochromic shift of the characteristic absorption band in the electronic spectra.

161 at the blue shift and increased width of the absorption band in the L135 mutants are due partly to ch

162 gths, matches well with the short-wavelength absorption band in the linear electronic spectrum and is

163 th flavins, and are characterized by a broad absorption band in the long wavelength region.

164 ludes appearance of an intervalence transfer absorption band in the near IR spectrum of the photochem

165 st time by its diagnostic (charge-resonance) absorption band in the near-IR region.

166 ns prepared herein exhibit a long-wavelength absorption band in the range 707-759 nm, providing tunab

167 Each bacteriochlorin exhibits a Q(y) absorption band in the range of 720-772 nm.

168 denced by the concomitant formation of a new absorption band in the UV/vis spectrum at 390 nm.

169 Detailed analysis of 1[n] revealed a broad absorption band in the visible region with maxima at 540

170 This compound has a major absorption band in the visible wavelength region with a

171 ree polysaccharides showed typical saccharic absorption bands in FT-IR.

172 Each chlorin exhibits dominant absorption bands in the blue and the red region (lambda

173 The CO adduct of Ngb displays two CO absorption bands in the IR spectrum, referred to as N(3)

174 between chemicals with strongly overlapping absorption bands in the mid-infrared.

175 TBPs and TNPs possess powerful absorption bands in the near-infrared (lambda = 610-710

176 igh solubility and exhibit remarkably strong absorption bands in the near-infrared region (790-950 nm

177 these rectangles reveal intense, asymmetric absorption bands in the near-infrared region, assigned a

178 dimeric species are characterized by intense absorption bands in the near-IR region that are diagnost

179 ll possessing a high fluorophore brightness, absorption bands in the near-UV and visible part of the

180 chromic shifts in both the Soret and visible absorption bands in the presence of Cc and an absorption

181 zation and shown to exhibit lowest energy UV absorption bands in the range 342-347 nm, confirming the

182 ot have any influence on the position of the absorption bands in the spectra.

183 that of their pyrimidine counterparts, with absorption bands in the UV or visible region and the emi

184 All of the compounds have intense absorption bands in the UV region assigned into (1)(pi -

185 the appearance of two new (charge-transfer) absorption bands in the UV-vis spectrum.

186 Their absorption bands in the vis region of the spectra are du

187 Theoretical calculations indicate that the absorption bands in the visible range can be tuned using

188 lorin, and BODIPY derivatives with different absorption bands in the visible region (503-668 nm) have

189 tense metal-to-ligand charge-transfer (MLCT) absorption bands in the visible region and room temperat

190 These compounds feature strong MLCT absorption bands in the visible region and strong red ph

191 The two outputs are the absorption bands in the visible region of the two colore

192 CYP3A4-Nanodiscs have absorption bands in the visible wavelength region, which

193 ut the lack of spectral data across telluric absorption bands in the wavelength region 2.5 to 2.9 mic

194 lecular orbitals that contribute to the main absorption bands in the XANES spectra.

195 ition, our calculations identify the exciton absorption bands in transient absorption spectra measure

196 tion into the p( perpendicular)(N)-->pi(N=C) absorption bands, indicating that the excited state is l

197 Excitation into the blue and red edge of the absorption band induces downhill and uphill energy flows

198 he dyes in a solution led to the increase in absorption band intensity in diffuse reflectance spectra

199 The lowest-energy absorption band is assigned as the transition from the a

200 The lowest energy absorption band is asymmetric with a weak low-energy sho

201 The singlet absorption band is completely formed 1 ps after the pump

202 ysis revealed that the characteristic 695 nm absorption band is shifted to 687 nm and reversed after

203 In the present study, this absorption band is used to selectively resonance enhance

204 of nonplanar deformations on the UV-visible absorption bands is then probed experimentally with a se

205 The silver cluster has a single violet absorption band (lambda(max) = 400 nm), and its single-s

206 ne) that exhibits an intense long-wavelength absorption band (lambda(max) = 516 nm, epsilon(516) = 48

207 It is shown that irradiation at the main absorption band leads to cyclobutane dimers (T<>Ts) and

208 mu(eff) = 3.80 mu(B), and assignment of its absorption bands leads to the ligand field parameters De

209 e excellent electronic properties but narrow absorption bands limit their utility in certain optoelec

210 The SEIRA enhancement increases and the absorption band line shape becomes more asymmetric as th

211 sion on irradiation into the long-wavelength absorption bands localized on the porphyrin.

212 pper atom are either type 1, with an intense absorption band near 600 nm, or type 2, with weak absorp

213 nstrated remarkably red-shifted intense Q(y) absorption bands observed in the range of 816-850 nm wit

214 , the unique charge-resonance (intervalence) absorption bands observed upon the one-electron oxidatio

215 Absorption band of BODIPY was tuned by installation of 0

216 sample absorbance is easily followed by the absorption band of localized surface plasmon resonance (

217 e at L135 and L247 shift the long-wavelength absorption band of P to higher energies.

218 We detected an absorption band of phenylborylene at 375 nm (S0 --> S2)

219 very intense surface plasmon resonance (SPR) absorption band of SNPs at 423 nm.

220 nches the fiber transmissions if there is an absorption band of the analyte overlapping with the tran

221 sults in its eventual merge with the intense absorption band of the dye around 500 nm in 3-Resf.

222 roximately 250 M(-1) cm(-1)) charge-transfer absorption band of the HMS.Fe(II).HPP complex.

223 ained if the laser wavelength matches the UV absorption band of the matrix in the solid state well.

224 polymer backbone, so that the lowest optical absorption band of the polymer has considerable intramol

225 The broad absorption band of the QDs in the visible region offers

226 ansmission measurement that would lead to an absorption band of the same intensity, is a more accurat

227 induced CD at the surface plasmon resonance absorption band of the silver nanoparticles.

228 g of Cu ions, the strong near-infrared (NIR) absorption band of the starting CuS NCs was essentially

229 The maximum for the Soret absorption band of this dimeric species is shifted to 39

230 ser flash photolysis experiments showing the absorption bands of 3-CN-NMQ(*) (lambdamax = 390 nm) and

231 significant changes in the characteristic IR absorption bands of all the bases and phosphate groups o

232 ecreasing the second transition enthalpy and absorption bands of amide I, II and III.

233 mposites exhibited broadened and red-shifted absorption bands of AuNRs in nIR region due to the plasm

234 ilbene chromophores has little effect on the absorption bands of capped hairpins.

235 is hindered by the superposition of similar absorption bands of carbonyl functional groups summing u

236 red/near-infrared wavelengths away from the absorption bands of hemoglobin.

237 erature range of 20-300 K as suggested by IR absorption bands of HOH bending and OH stretching modes

238 , time-resolved perturbations of the visible absorption bands of L29F and V68L deoxyMb generated afte

239 romic and hypsochromic shifts in the maximum absorption bands of MTX after interaction with DNA.

240 of DNA and the overlap of DNA bands with the absorption bands of other biochemical components.

241 the large red shifts seen in the UV-visible absorption bands of peripherally crowded nonplanar porph

242 3 is consistent with electrochromic shift of absorption bands of the Chl a pigments in the vicinity o

243 Independent VTVH-MCD studies on multiple absorption bands of the complex yield D = -14(3) cm(-1),

244 The relatively weak absorption bands of the delocalized polaron in the visib

245 hemoglobin Soret absorption band and to the absorption bands of the dyes were used to demarcate the

246 orm disks with large linear dichroism in the absorption bands of the dyes.

247 Excitation into these absorption bands of the Fe(II)TauD(alpha-KG) complex (Ta

248 resulting in a significant red shift of the absorption bands of the naphthalenic chromophore.

249 The absorption bands of the PA aliphatic backbone at 2902, 2

250 Dual absorption bands of the phenolic moiety indicate a doubl

251 incident light is far away from the optical absorption bands of the protein, a approximately 0.008 d

252 emission of YFP and the visible-region (QX) absorption bands of the RC allow energy transfer via a F

253 The FTIR spectroscopy showed the absorption bands of the stretching modes of Zn-O between

254 Incidentally, the absorption bands of water increased resulting from surfa

255 n of nanosecond laser induced transient dual absorption bands, one in the bandgap (TA(1)) and another

256 However, their absorption bands provide limited coverage in the visible

257 can have (bacterio)chlorophyll Q(y) antenna absorption bands ranging from approximately 650 to appro

258 Amide I, amide II, and other infrared absorption bands, recorded from single bacteriorhodopsin

259 balamin at 520 nm in the low-lying alphabeta absorption band results in bond homolysis proceeding via

260 Changes in the retinal absorption band reveal two transient retinal-protein int

261 A large decrease in the FTIR absorption band's magnitude was observed in the hydrocar

262 le their fluorescence is overlapped with the absorption band(s) of the core metalloporphyrin, ensurin

263 erials on the basis of spectral coverage and absorption band shape.

264 The distinct origins of the absorption band shifts associated with the formation of

265 3d --> corrin pi* transitions and by visible absorption bands similar to the corrin pi-->pi* transiti

266 pid and irreversible loss of anthracyclines' absorption bands, suggesting oxidative degradation of th

267 omic behavior of Ir(III)-corrole Soret and Q absorption bands suggests that the lowest singlet excite

268 Ar(4)(MeO)(8)TNPs exhibit more red-shifted absorption bands than Ar(4)TNPs and differ dramatically

269 ppR'(496) has an absorption band that is shifted to shorter wavelengths b

270 O(-), and H2PO4(-) induced a new red-shifted absorption band that was attributed to a deprotonation p

271 The data shows a number of absorption bands that are assigned to one- and two-phono

272 In solution, 3a-c show strong disq--based absorption bands that are invariant across the halide se

273 s in length contained vestigial neutral (VN) absorption bands that arise from neutral parts of the ch

274 heir optical spectra: All show lowest energy absorption bands that correspond to an alpha-homo (highe

275 ndolines with varying basicities and tunable absorption bands that extend to the near-infrared region

276 eory of spectroscopy to fit the two observed absorption bands that have resolved vibronic structure.

277 spite the spectral red-shift of their lowest absorption band, the fluorescence quantum yields increas

278 Upon excitation into any of these four absorption bands, the (C(5)Me(5))(2)U[-N=C(Ph)(R)](2) co

279 citation into the lowest-energy ligand-field absorption band; the time constant is found to be indepe

280 l porphyrinoid photoproducts possess intense absorption bands throughout the visible spectral region,

281 witnessed by a strong red-shift of the probe absorption bands, thus allowing the generation of dichro

282 ieved by spectral matching of the sensitizer absorption band to different types of localized photon m

283 tion constant and evaluation of intervalence absorption bands using appropriate theoretical models yi

284 Characteristic optical absorption bands, vibrational frequencies, and hyperfine

285 Shifts in the absorption band wavelength and intensity as a function o

286 Shifts of 4-23 nm in the Q(y) absorption band were observed in seven mutants with sing

287 No new absorption bands were observed for either methionine or

288 splays vibronic structure in the lambda(max) absorption band, whereas the other pigments display full

289 P) can be excited at the red edge of the Trp absorption band which allows normalisation of the emissi

290 It is preceded by a strong and broad absorption band, which is tentatively assigned to excite

291 The caged compound has a major absorption band with a maximum at 390 nm (epsilon(390) =

292 The caged compound has a major absorption band with a maximum at 390 nm (epsilon390 = 1

293 we correlate a shift in the chlorophyll red absorption band with deformation of its tetrapyrrole mac

294 p-nitrophenyl phosphate, exhibits a visible absorption band with lambda(max) at 570 nm.

295 A transient absorption band with maximum amplitude near 600 nm was d

296 d LMCT excited state has a single CN-stretch absorption band with no anisotropy.

297 m indicates heterogeneity of the red pigment absorption band with two broad homogeneous transitions a

298 crocycles exhibited bathochromically shifted absorption bands with a distinct change in the color of

299 We detected prominent H2O absorption bands with a maximum base-to-peak amplitude o

300 ompounds and reveal at least two significant absorption bands within the region 420-550 nm.