ライフサイエンスコーパス: photodissociation

1 hotochemistry, including photoexcitation and photodissociation.

2 e order of approximately 1 s with respect to photodissociation.

3 tein dynamics following carbon monoxide (CO) photodissociation.

4 e dependence of the protein relaxation after photodissociation.

5 m the importance of self-shielding during CO photodissociation.

6 nsight into the mechanism of the two-channel photodissociation.

7 .6 mL mol(-1)) that occurs within 50 ns upon photodissociation.

8 tion spectrum caused by water entry after CO photodissociation.

9 r entry several hundred nanoseconds after CO photodissociation.

10 al time, from 5 ns to 80 micros after ligand photodissociation.

11 nate and bimolecular CO recombination, after photodissociation.

12 d be formed by both thermal dissociation and photodissociation.

13 rotein structure that occur following ligand photodissociation.

14 ed instrument facilitates activated electron photodissociation.

15 dissociation (EThcD) and 213 nm ultraviolet photodissociation (213 nm UVPD) to provide more comprehe

16 We report the first application of UV/Vis photodissociation action spectroscopy for the structure

17 Here we achieve this control using photodissociation, an approach that encodes a wealth of

18 isotopic effects during carbon monoxide (CO) photodissociation and argued that self-shielding in CO w

19 and photoacoustic calorimetry studies of CO photodissociation and bimolecular rebinding to neuroglob

20 etailed experiments on formaldehyde (H(2)CO) photodissociation and determined fully correlated quantu

21 and protein relaxation after carbon monoxide photodissociation and during rebinding.

22 e of the traditional quasiclassical model of photodissociation and instead are accurately described b

23 Reported herein is a facile method employing photodissociation and mass spectrometry to localize site

24 With variation of the time between photodissociation and orthogonal extraction in the TOF s

25 By combination of photodissociation and postsource decay (PSD) spectra, th

26 (PAC), we have characterized carbon monoxide photodissociation and rebinding to two forms of the heme

27 Escape of carbon via CO photodissociation and sputtering enriches heavy carbon (

28 aser shot UVPD discriminates between primary photodissociation and subsequent fragmentation of fragme

29 tially induced by (*)OH formed from FeOH(2+) photodissociation and was inhibited 2-fold by dissolved

30 ntensity at hundreds of nanoseconds after CO photodissociation, and this was followed by recovery in

31 This scenario also supports N2 photodissociation as the cause of the large nitrogen iso

32 Photodissociation at 2.5 eV leads to one-atom caging and

33 ched in (17)O and (18)O than that from ozone photodissociation at lower altitudes.

34 Ab initio quantification of the photodissociations at play fills a critical data void in

35 zed Hg(I) and Hg(II) species postulate their photodissociation back to Hg(0) as a crucial step in the

36 Here, we present resonant infrared photodissociation based on diagnostic sulfate and phosph

37 ructose proves to be an excellent matrix for photodissociation because [M + H]+ ions are formed with

38 henated LC-MS methods, and their predictable photodissociation behavior allows de novo identification

39 f sequences optimized for strand binding and photodissociation, both useful for optogenetic applicati

40 We elucidated the mechanism of strand photodissociation by measuring the dependence of its rat

41 es has been the short time scale for ammonia photodissociation by solar ultraviolet light.

42 Previous cryogenic (80 K) FTIR CO photodissociation difference results were obtained for c

43 o pond seepage during wet periods, and to UV photodissociation during dry periods, mean that the synt

44 Y(0(+)), and Z(0(+)) states of IBr, and the photodissociation dynamics are tracked with an attosecon

45 Ion imaging reveals distinct photodissociation dynamics for propanal cations initiall

46 The photodissociation dynamics of 1,3-butadiene at 193 nm ha

47 e-state, surface hopping calculations of the photodissociation dynamics of formaldehyde are reported

48 can provide guidance in this matter, and the photodissociation dynamics of thermal NCNO to form CN an

49 e, and multidimensional tunneling, of phenol photodissociation dynamics.

50 action products to reveal new aspects of the photodissociation dynamics.

51 Photodissociation efficiencies of approximately 100% and

52 carried out at the atmospherically relevant photodissociation energies led to recombination of OH an

53 Ligand photodissociation experiments are used to measure the pr

54 A series of CO photodissociation experiments at the Advanced Light Sour

55 etry, we discovered a unique photoionization-photodissociation fragmentation process for polymers con

56 C(120)O(2) undergoes photodissociation from its triplet state to regenerate m

57 me-resolved absorption measurements after CO photodissociation from unfolded Fe(II)(CO)-Cyt c' confir

58 Reversible complementation is desirable, but photodissociation has too low of an efficiency (quantum

59 Photoactivation and photodissociation have long proven to be useful tools in

60 experimental results provide support for CO photodissociation having caused the oxygen isotope ratio

61 ost peptide ions did not undergo significant photodissociation; however, in the low pressure cell pep

62 in nuclear physics, and photoassociation and photodissociation in biology and chemistry.

63 the protein quake after carbon monoxide (CO) photodissociation in myoglobin.

64 effect of arachidonic acid, which abolished photodissociation in the absence of ethanol but had no e

65 we report time-dependent calculations of CO photodissociation in the cooler surface region of a turb

66 me and enthalpy changes were observed for CO photodissociation in the presence of the substrate, 2,4-

67 Peptide photodissociation in this apparatus yielded fragments si

68 mer of a bisdithiazolyl radical leads to its photodissociation into a pair of pi-radicals.

69 des containing the AF350 chromophore undergo photodissociation into extensive arrays of b- and y-type

70 bsorption spectroscopy, multiphoton infrared photodissociation (IRMPD) action spectroscopy, and densi

71 Infrared multiphoton photodissociation (IRMPD) is combined with stored wave f

72 3-)(H(2)O)n were investigated using infrared photodissociation (IRPD) kinetics, spectroscopy, and com

73 Infrared photodissociation (IRPD) spectra between approximately 2

74 Ensemble infrared photodissociation (IRPD) spectra in the hydrogen stretch

75 Ensemble infrared photodissociation (IRPD) spectra in the hydrogen stretch

76 r molecules were investigated using infrared photodissociation (IRPD) spectroscopy and blackbody infr

77 ted heptylamine are investigated by infrared photodissociation (IRPD) spectroscopy and computational

78 derivatives are investigated using infrared photodissociation (IRPD) spectroscopy and kinetics as we

79 Results from infrared photodissociation (IRPD) spectroscopy and kinetics of si

80 ister series are investigated using infrared photodissociation (IRPD) spectroscopy.

81 pectrometry combined with two-color infrared photodissociation (IRPD) spectroscopy.

82 ne, complex 1) using helium tagging infrared photodissociation (IRPD), absorption, and magnetic circu

83 The results show that strand photodissociation is a two-step process involving light-

84 Our data show that CO photodissociation is associated with an endothermic (Del

85 indicates that the tertiary relaxation after photodissociation is nearly complete within 10 ns, as is

86 ed deactivation is suppressed and protolytic photodissociation is observed.

87 MALDI-TOF photodissociation is then used to selectively sequence t

88 Photodissociation kinetic data for MABAH(+).(H2O)6 indic

89 After photodissociation, ligand rebinding to myoglobin exhibit

90 The measured photodissociation mass spectra exhibit isoform-specific

91 Photodissociation mass spectra obtained at wavelengths r

92 Photodissociation mass spectra of fatty acids conjugated

93 Here, we employ 213 nm ultraviolet photodissociation mass spectrometry (UVPD-MS) for struct

94 Photodissociation mass spectrometry combines the ability

95 esolution and high-mass-accuracy ultraviolet photodissociation mass spectrometry for the most in-dept

96 The scope and breadth of photodissociation mass spectrometry have increased subst

97 It is based on ultraviolet photodissociation mass spectrometry of cryogenically coo

98 w focuses on many of the key developments in photodissociation mass spectrometry over the past decade

99 A combination of photodissociation mass spectrometry over the ultraviolet

100 loped sulfotransferase assay and ultraviolet photodissociation mass spectrometry to demonstrate that

101 out by applying two-color, infrared-infrared photodissociation mass spectrometry to the D(3)O(+).(HDO

102 derstand the ground state properties and the photodissociation mechanism of SiH2OO, a silicon analogu

103 However, the significance of these photodissociation mechanisms on atmospheric Hg chemistry

104 ental evidence for the C + O2 channel in CO2 photodissociation near the energetic threshold of the C(

105 ly they are directed to the TOF source where photodissociation occurs and product ions are extracted

106 ed experimentally and theoretically in which photodissociation of 1D metal halide chains followed by

107 evolution of molecular chirality during the photodissociation of 2-iodobutane.

108 heme iron on microsecond time scales, after photodissociation of a carbon monoxide ligand from the h

109 nvestigation of nonadiabatic dynamics during photodissociation of a complex of iodine monobromide ani

110 Photodissociation of a non-native carbon-iodine bond inc

111 observation of product ions following 157 nm photodissociation of a singly charged tryptic peptide io

112 Photodissociation of all complexes occurs by the elimina

113 was used to monitor protein relaxation after photodissociation of aqueous HbCO complex under osmotic

114 volution of organic aerosol initiated by the photodissociation of aqueous iron(III) oxalate complexes

115 Ultraviolet photodissociation of BAH-cross-linked peptides also yiel

116 Photodissociation of carbon dioxide (CO2) has long been

117 4% relative to water, cannot be explained by photodissociation of carbon monoxide and is instead attr

118 Ligand photodissociation of carboxymyoglobin (MbCO) induces a s

119 oupled protein structures in response to the photodissociation of CO from heme Fe and its subsequent

120 ox centers of cytochrome c oxidase following photodissociation of CO from the CO-bound mixed valence

121 The folding of reduced cyt c induced by photodissociation of CO from the CO-bound unfolded prote

122 Surprisingly, photodissociation of CO from the mixed valence form of t

123 After photodissociation of CO from the partially denatured fer

124 ificantly from those measured previously for photodissociation of CO from the structural homologue my

125 Isotope-selective photodissociation of CO in the innermost solar nebula mi

126 osecond and microsecond time-scale following photodissociation of CO ligands.

127 ion with change in spin state of the iron by photodissociation of CO or perturbation of the CuB coord

128 ht Source show that vacuum ultraviolet (VUV) photodissociation of CO produces large wavelength-depend

129 Exploiting earlier studies on photodissociation of cut s10 from GFP, ratiometric prote

130 New experimental results on VUV photodissociation of dipeptides (protonated Ala_Arg and

131 o study singlet diphenylcarbene generated by photodissociation of diphenyldiazomethane with a UV puls

132 Photodissociation of ethylene sulfide at 193 nm has been

133 Photodissociation of fully reduced, carbonmonoxy cytochr

134 activation using UV laser pulses, efficient photodissociation of glycopeptides is achieved with prod

135 of reactions with HBpin and PhSiH3 show that photodissociation of H2 from 1 occurs prior to substrate

136 Hot-electron-induced photodissociation of H2 was demonstrated on small Au nan

137 hase species in the solar nebula, and hence, photodissociation of H2S by solar vacuum UV (VUV) photon

138 VUV photodissociation of H2S takes place through several pre

139 Here, we focus on the photodissociation of ICN in the (1) Pai(1) excited state

140 These results suggest that photodissociation of iron(III) oxalate can lead to the f

141 comparison of product distributions from the photodissociation of jet and thermal ensembles at identi

142 ion pair products of the vacuum ultraviolet photodissociation of methyl chloride.

143 Simulations show that photodissociation of methyl hydroperoxide, CH(3)OOH, on

144 Advanced Light Source (ALS), we measured the photodissociation of molecular nitrogen (N(2)) with vacu

145 The measured enrichment range in photodissociation of N2, plausibly explains the range of

146 served at the inner transition state for the photodissociation of NCNO at 514, 520, and 526 nm.

147 Here, we present an imaging study of the photodissociation of nitrobenzene with state-specific de

148 Photodissociation of NO leaves the sample in the dehydra

149 the first step of the main mechanism is the photodissociation of NO2, which then recombines with the

150 esolved spectra of photoproducts from ligand photodissociation of oxyhemoglobin are measured in the S

151 (SO(4)) that, in turn, are derived from the photodissociation of persulfate anions (S(2)O(8)(2-)) in

152 ultrafast reaction dynamics following 295-nm photodissociation of Re2CO10 were studied experimentally

153 lution of this absorption band subsequent to photodissociation of six coordinate ferrous hemoglobin o

154 ted, the quantum efficiency of light-induced photodissociation of split GFPs is low.

155 ne moiety can be leveraged for site specific photodissociation of the backbone.

156 of tyrosine to iodo-tyrosine followed by UV photodissociation of the carbon-iodine bond can be used

157 gnetic circular dichroism spectroscopy after photodissociation of the CO complexes of unfolded protei

158 pectrometric multichannel analyzer following photodissociation of the cobalt complex.

159 esolved optical spectra following nanosecond photodissociation of the heme-carbon monoxide complex.

160 oinduced linkage isomerism (MS1 and MS2) and photodissociation of the metal-NO bond in SNP highlights

161 analysis reveals that photoisomerization and photodissociation of the metal-NO moiety are competing p

162 pproximately 10 picoseconds) with N2 and the photodissociation of the N2:O2 dimer produce NOx in the

163 nd transient absorption changes following NO photodissociation of the proximal 5c-NO AXCP complex.

164 state, and measured v-j correlations in the photodissociation of thermal NCNO are presented.

165 However, photodissociation of this NO2 unexpectedly produced NO m

166 It has previously been shown that photodissociation of tryptic peptide ions with 157 nm li

167 calculations, we propose a mechanism for the photodissociation of UVR8 that consists of three steps:

168 Photodissociation of water at a wavelength of 121.6 nano

169 f an oxygenic prebiotic atmosphere caused by photodissociation of water vapor followed by escape of h

170 "super rotors", from the vacuum ultraviolet photodissociation of water.

171 In THF compound I undergoes a reversible photodissociation, potentially due to CO loss.

172 principles study of the carbon dioxide (CO2) photodissociation process in the 150- to 210-nm waveleng

173 tion of the most recent experiments that the photodissociation process is dominated by tunneling.

174 Model studies of the ligand photodissociation process of carboxymyoglobin have been

175 nd bending coordinate play a key role in the photodissociation process.

176 very effective in rationalizing the observed photodissociation processes.

177 example of resonance-mediated control of the photodissociation processes.

178 To detect photodissociation product ions having axially divergent

179 to observe time-dependent vacuum ultraviolet photodissociation product ions.

180 was suggested by a marginal detection of the photodissociation product of water, hydroxyl, but could

181 Other photodissociation products including cyanide ion, Prussi

182 seemingly very different peptide binding and photodissociation properties of split proteins involving

183 In the analysis of various tryptic peptides, photodissociation provided much more sequence informatio

184 pecies-specific differences in both the 8-ns photodissociation quantum yield and the rebinding kineti

185 ovide potential strategies for improving the photodissociation quantum yield.

186 The (t approximately 0) photodissociation quantum yields (Y(0)) of MbNO and MbO(

187 ntial energy surface (PES) diagram along the photodissociation reaction coordinate.

188 We examine the photodissociation reaction of trimethylamine and identif

189 size and ring arrangements, which suggested photodissociation, recombination, and ring re-arrangemen

190 The photodissociation reveals both the presence and location

191 based on the m/z of each precursor ion, the photodissociation setup was seamlessly automated with th

192 Infrared photodissociation spectra of M(+)(H2O)(x=2-5) (approxima

193 Infrared photodissociation spectra of M(+)(H2O)(x=2-5)Ar (with ef

194 We present infrared photodissociation spectra of two protonated peptides tha

195 High-quality photodissociation spectra were obtained with as little a

196 Comparisons of the photodissociation spectra with spectra calculated for lo

197 ound molecules through their radio-frequency photodissociation spectra; these probe the molecular wav

198 Low-temperature photodissociation spectrophotometry revealed that neithe

199 es attached were investigated using infrared photodissociation spectroscopy (IRPD), blackbody infrare

200 structure of [VPO4](*+) is determined by IR photodissociation spectroscopy and compared to that of [

201 n)(-), n <= 200, at T = 80 K are obtained by photodissociation spectroscopy and compared with simulat

202 spray ionization (ESI) coupled with infrared photodissociation spectroscopy and computational chemist

203 l, I, SF6; n = 0-5) were studied by infrared photodissociation spectroscopy and computational chemist

204 f-flight mass spectrometer by infrared laser photodissociation spectroscopy in the C-H stretch region

205 light spectrometer and studied with IR laser photodissociation spectroscopy in the carbonyl-stretchin

206 Infrared photodissociation spectroscopy in the N-N stretching reg

207 Infrared photodissociation spectroscopy is reported for mass-sele

208 IR photodissociation spectroscopy of mass-selected [Bi(CO2

209 Examples span from ultraviolet and infrared photodissociation spectroscopy of model reaction interme

210 tallization of (H2O)n clusters with infrared photodissociation spectroscopy of size-selected La(3+)(H

211 rometer and investigated with infrared laser photodissociation spectroscopy using the method of "tagg

212 niques, including isotope labeling, infrared photodissociation spectroscopy, gas-phase hydrogen/deute

213 o 15 water molecules attached using infrared photodissociation spectroscopy, laser-induced dissociati

214 The infrared photodissociation spectrum of Eu(H(2)O)(119-124)(3+) ind

215 Here, to unambiguously determine the post-photodissociation steps involving CO, we have monitored

216 This work presents a photodissociation study of the diamondoid adamantane usi

217 Thermally assisted infrared multiphoton photodissociation (TA-IRMPD) provides an effective means

218 he basic BAH-moiety underwent more efficient photodissociation than the peptide ions with sequestered

219 Before photodissociation, the carbonyl (C=O)-stretching frequen

220 decay within less than 500 fs, revealing the photodissociation to achiral products.

221 sorbing chromophore that undergoes efficient photodissociation to give iron(II) and the carbon dioxid

222 applications that illustrate the ability of photodissociation to produce rich fragmentation patterns

223 rimary product ions also underwent efficient photodissociation to yield singly charged secondary prod

224 The utility of 193-nm ultraviolet photodissociation (UVPD) and 10.6-mum infrared multiphot

225 on induced dissociation (CID) or ultraviolet photodissociation (UVPD) and a mass analysis (MS2 scan).

226 separations with MS(3) utilizing ultraviolet photodissociation (UVPD) and higher-energy collisional d

227 view will showcase the impact of ultraviolet photodissociation (UVPD) as a frontier strategy for gene

228 dissociation (ETD) combined with ultraviolet photodissociation (UVPD) at 193 nm for analysis of intac

229 Ultraviolet photodissociation (UVPD) at 193 nm is compared to collis

230 Here, we investigate the use of ultraviolet photodissociation (UVPD) at 213 nm to measure deuterium

231 ctivated dissociation (EAD), and ultraviolet photodissociation (UVPD) at 266 nm.

232 Only the tagged peptides undergo ultraviolet photodissociation (UVPD) at 351 nm, as demonstrated for

233 Ultraviolet photodissociation (UVPD) at 355 nm was used to rapidly i

234 h successful characterization by ultraviolet photodissociation (UVPD) for MS/MS analysis in a middle-

235 Here, we present the use of ultraviolet photodissociation (UVPD) for the characterization of dou

236 s phase was undertaken by 193 nm ultraviolet photodissociation (UVPD) for the characterization of hig

237 ere is the application of 193 nm ultraviolet photodissociation (UVPD) for top down identification and

238 pectrometer can be extended with ultraviolet photodissociation (UVPD) fragmentation, complete with sy

239 Ultraviolet photodissociation (UVPD) generates a multitude of sequen

240 In contrast, 193 nm ultraviolet photodissociation (UVPD) generates a wide array of produ

241 Ultraviolet photodissociation (UVPD) has recently been introduced as

242 Ultraviolet photodissociation (UVPD) has shown great utility for loc

243 ssociation (CID) followed by 193 ultraviolet photodissociation (UVPD) implemented on an Orbitrap Fusi

244 Here, we explore ultraviolet photodissociation (UVPD) implemented on an Orbitrap mass

245 In the present work, 193 nm ultraviolet photodissociation (UVPD) implemented on an Orbitrap mass

246 Furthermore, our use of 193-nm ultraviolet photodissociation (UVPD) improves spectral coverage of t

247 Here we implement ultraviolet photodissociation (UVPD) in an online liquid chromatogra

248 ibe the implementation of 193 nm ultraviolet photodissociation (UVPD) in an Orbitrap mass spectromete

249 omatic label for enhanced 193 nm ultraviolet photodissociation (UVPD) is demonstrated using a dual el

250 C-MS/MS platform based on 351 nm ultraviolet photodissociation (UVPD) is presented for the selective

251 Ultraviolet photodissociation (UVPD) is used to analyze the resultin

252 Ultraviolet photodissociation (UVPD) mass spectrometry (MS) was used

253 light-emitting diodes (LEDs) for ultraviolet photodissociation (UVPD) mass spectrometry is reported.

254 Top-down ultraviolet photodissociation (UVPD) mass spectrometry is used to tr

255 A chemical probe/ultraviolet photodissociation (UVPD) mass spectrometry strategy for

256 Ultraviolet photodissociation (UVPD) mass spectrometry was used to c

257 MTX were characterized by 193 nm ultraviolet photodissociation (UVPD) mass spectrometry.

258 ate the utility of negative mode ultraviolet photodissociation (UVPD) MS for the characterization of

259 Ultraviolet photodissociation (UVPD) of chromophore-modified peptide

260 Ultraviolet photodissociation (UVPD) of gas-phase proteins has attra

261 Vacuum ultraviolet laser photodissociation (UVPD) of peptide ions leads to unusua

262 Ultraviolet photodissociation (UVPD) of peptides derivatized by sele

263 Here, we implemented ultraviolet photodissociation (UVPD) on an Orbitrap mass spectromete

264 Ultraviolet photodissociation (UVPD) produces complementary fragment

265 Ultraviolet photodissociation (UVPD) produces rich and informative f

266 t MS/MS analysis by using 193 nm ultraviolet photodissociation (UVPD) results in enhanced formation o

267 e sequence and structure showing ultraviolet photodissociation (UVPD) spectra of mass and mobility se

268 Here, ultraviolet photodissociation (UVPD) strategies for phospholipid cha

269 sine cross-linked peptides under ultraviolet photodissociation (UVPD) tandem mass spectrometry (MS/MS

270 backbone fragmentation by 193-nm ultraviolet photodissociation (UVPD) to determine the linkage patter

271 workflow utilizing native MS and ultraviolet photodissociation (UVPD) to map the antigenic determinan

272 PTR was combined with ultraviolet photodissociation (UVPD) to probe the degree of structur

273 e of targeted middle-down 193 nm ultraviolet photodissociation (UVPD) to provide detailed primary seq

274 The capabilities of 193 nm ultraviolet photodissociation (UVPD) to yield informative backbone s

275 Ultraviolet photodissociation (UVPD) using 193 nm photons has proven

276 ionization in the negative mode, ultraviolet photodissociation (UVPD) was applied for peptide sequenc

277 ctrometry combined with top-down ultraviolet photodissociation (UVPD) was employed to investigate the

278 ure dissociation (ECD) or 193 nm ultraviolet photodissociation (UVPD) were attributed to structural c

279 ted the implementation of 193 nm ultraviolet photodissociation (UVPD) within the ion cyclotron resona

280 benium ion generation to trigger ultraviolet photodissociation (UVPD), an alternate high-energy depos

281 tilizing a combination of 193 nm ultraviolet photodissociation (UVPD), electron-transfer dissociation

282 also compared to that of 193 nm ultraviolet photodissociation (UVPD), which allowed us to explore th

283 re dissociation (ECD) and 157 nm ultraviolet photodissociation (UVPD).

284 ed dissociation (CID) and 351 nm ultraviolet photodissociation (UVPD).

285 d peptides susceptible to 351 nm ultraviolet photodissociation (UVPD).

286 es that is cleavable upon 266 nm ultraviolet photodissociation (UVPD).

287 ollisional dissociation (HCD) or ultraviolet photodissociation (UVPD).

288 owed by in-cell fragmentation by ultraviolet photodissociation (UVPD).

289 per thousand in product NH3, depending upon photodissociation wavelength.

290 At atmospherically relevant photodissociation wavelengths the OH and CH(3)O photofra

291 Rebinding of CO and of Cys-52 following CO photodissociation were independently monitored via time-

292 ollision dissociation and 213 nm ultraviolet photodissociation were utilized to provide complementary

293 Photodissociation with 157 nm light was implemented in a

294 Photodissociation with 266 nm light yields homolytic cle

295 we have monitored the CO vibration following photodissociation with step-scan FT-IR spectroscopy.

296 oir can be generated through carbon monoxide photodissociation without self-shielding.

297 n reservoir can thus be generated through CO photodissociation without self-shielding.

298 transfer dissociation (NETD), or extreme UV photodissociation (XUV-PD).

299 Combining the photodissociation yields across this spectral window pro

300 hermometry technique that relies on relative photodissociation yields.