Difference between revisions of "Butyl PBD"
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| ImageFile = Butyl PBD.png | | ImageFile = Butyl PBD.png | ||
| IUPACName = 2-(4-''tert''-Butylphenyl)-5-(4-phenylphenyl)-1,3,4-oxadiazole | | IUPACName = 2-(4-''tert''-Butylphenyl)-5-(4-phenylphenyl)-1,3,4-oxadiazole | ||
| + | | OtherNames = 2-(4-''tert''-Butylphenyl)-5-(4-biphenylyl)-1,3,4-oxadiazole<br/>2-(4-Biphenylyl)-5-(4-''tert''-butylphenyl)-1,3,4-oxadiazole | ||
| Section1 = {{Chembox Identifiers | | Section1 = {{Chembox Identifiers | ||
| − | | InChI=1/C24H22N2O/c1-24(2,3)21-15-13-20(14-16-21)23-26-25-22(27-23)19-11-9-18(10-12-19)17-7-5-4-6-8-17/h4-16H,1-3H3 | + | | InChI={{InChIwrap|1/C24H22N2O/c1-24(2,3)21 -15-13-20(14-16-21)23-26-25-22( 27-23)19-11-9-18(10-12-19)17-7 -5-4-6-8-17/h4-16H,1-3H3}} |
| − | | StdInChI=1S/C24H22N2O/c1-24(2,3) | + | | StdInChI={{InChIwrap|1S/C24H22N2O/c1-24(2,3)2 1-15-13-20(14-16-21)23-26-25-22 (27-23)19-11-9-18(10-12-19)17- 7-5-4-6-8-17/h4-16H,1-3H3}} |
| InChIKey = XZCJVWCMJYNSQO-UHFFFAOYAT | | InChIKey = XZCJVWCMJYNSQO-UHFFFAOYAT | ||
| StdInChIKey = XZCJVWCMJYNSQO-UHFFFAOYSA-N | | StdInChIKey = XZCJVWCMJYNSQO-UHFFFAOYSA-N | ||
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}} | }} | ||
| − | '''Butyl PBD''' or '''b-PBD''' is a [[Fluorescence|fluorescent]] organic compound used in the [[Liquid Scintillator Neutrino Detector]] at [[Los Alamos National Laboratory]], USA.<ref>{{citation | title = The Liquid Scintillator Neutrino Detector and LAMPF Neutrino Source | first1 = C. | last1 = Athanassopoulos | first2 = L. B. | last2 = Auerbach | first3 = D. | last3 = Bauer | first4 = R. D. | last4 = Bolton | first5 = R. L. | last5 = Burman | first6 = I. | last6 = Cohen | first7 = D. O. | last7 = Caldwell | first8 = B. D. | last8 = Dieterle | first9 = J. B. | last9 = Donahue | A. M. Eisner | + | '''Butyl PBD''' or '''b-PBD''' is a [[Fluorescence|fluorescent]] organic compound used in the [[Liquid Scintillator Neutrino Detector]] (LSND) at [[Los Alamos National Laboratory]], USA.<ref name="LSND">{{citation | title = The Liquid Scintillator Neutrino Detector and LAMPF Neutrino Source | first1 = C. | last1 = Athanassopoulos | first2 = L. B. | last2 = Auerbach | first3 = D. | last3 = Bauer | first4 = R. D. | last4 = Bolton | first5 = R. L. | last5 = Burman | first6 = I. | last6 = Cohen | first7 = D. O. | last7 = Caldwell | first8 = B. D. | last8 = Dieterle | first9 = J. B. | last9 = Donahue | first10 = A. M. | last10 = Eisner | first11 = A. | last11 = Fazely | first12 = F. J. | last12 = Federspiel | first13 = G. T. Garvey | last13 = M. Gray | first14 = R. M. | last14 = Gunasingha | first15 = V. | last15 = Highland | first16 = R. | last16 = Imlay | first17 = K. | last17 = Johnston | first18 = H. J. | last18 = Kim | first19 = W. C. | last19 = Louis | first20 = A. | last20 = Lu | first21 = J. | last21 = Margulies | first22 = G. B. | last22 = Mills | first23 = K. | last23 = McIlhany | first24 = W. | last24 = Metcalf | first25 = R. A. | last25 = Reeder | first26 = V. | last26 = Sandberg | first27 = M. | last27 = Schillaci | first28 = D. | last28 = Smith | first29 = I. | last29 = Stancu | first30 = W. | last30 = Strossman | first31 = R. | last31 = Tayloe | first32 = G. J. | last32 = Van Dalen | first33 = W. | last33 = Vernon | first34 = Y-X. | last34 = Wang | first35 = D. H. | last35 = White | first36 = D. | last36 = Whitehouse | first37 = D. | last37 = Works | first38 = Y. | last38 = Xiao | first39 = S. | last39 = Yellin | journal = Nucl. Instrum. Meth. A | volume = 388 | pages = 149–72 | year = 1997 | doi = 10.1016/S0168-9002(96)01155-2 | arxiv = nucl-ex/9605002v1}}.</ref> |
| + | |||
| + | The fluorescent emission of b-PBD is at ''λ''<sub>em</sub> = 364 nm for excitation at ''λ''<sub>ex</sub> = 305 nm (in [[ethanol]] solution).<ref>{{citation | title = B8378 2-(4-tert-Butylphenyl)-5-(4-biphenylyl)-1,3,4-oxadiazole ≥99% | url = http://www.sigmaaldrich.com/catalog/ProductDetail.do?D7=0&N5=Product%20No.|BRAND_KEY&N4=B8378|Sigma&N25=0&QS=ON&F=SPEC | publisher = Sigma-Aldrich | accessdate = 2010-05-22}}.</ref> As a scintillant in the LSND, it was used at a concentration of 31 mg/l (87 µmol/l) dissolved in [[mineral oil]].<ref name="LSND"/> | ||
==References== | ==References== | ||
| Line 23: | Line 26: | ||
==External links== | ==External links== | ||
| + | {{wikipedia|Butyl PBD}} | ||
[[Category:Oxadiazoles]] | [[Category:Oxadiazoles]] | ||
{{CC-BY-3.0}} | {{CC-BY-3.0}} | ||
Latest revision as of 07:04, 23 May 2010
| Butyl PBD | |
|---|---|
| |
| IUPAC name | 2-(4-tert-Butylphenyl)-5-(4-phenylphenyl)-1,3,4-oxadiazole |
| Other names | 2-(4-tert-Butylphenyl)-5-(4-biphenylyl)-1,3,4-oxadiazole 2-(4-Biphenylyl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazole |
| Identifiers | |
| InChI | InChI=1/C24H22N2O/c1-24(2,3)21 -15-13-20(14-16-21)23-26-25-22( 27-23)19-11-9-18(10-12-19)17-7 -5-4-6-8-17/h4-16H,1-3H3 |
| InChIKey | XZCJVWCMJYNSQO-UHFFFAOYAT |
| Standard InChI | InChI=1S/C24H22N2O/c1-24(2,3)2 1-15-13-20(14-16-21)23-26-25-22 (27-23)19-11-9-18(10-12-19)17- 7-5-4-6-8-17/h4-16H,1-3H3 |
| Standard InChIKey | XZCJVWCMJYNSQO-UHFFFAOYSA-N |
| CAS number | [] |
| EC number | |
| ChemSpider | |
| Properties | |
| Chemical formula | C24H22N2O |
| Molar mass | 354.44 g mol−1 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
Butyl PBD or b-PBD is a fluorescent organic compound used in the Liquid Scintillator Neutrino Detector (LSND) at Los Alamos National Laboratory, USA.[1]
The fluorescent emission of b-PBD is at λem = 364 nm for excitation at λex = 305 nm (in ethanol solution).[2] As a scintillant in the LSND, it was used at a concentration of 31 mg/l (87 µmol/l) dissolved in mineral oil.[1]
References
- ↑ 1.0 1.1 Athanassopoulos, C.; Auerbach, L. B.; Bauer, D.; Bolton, R. D.; Burman, R. L.; Cohen, I.; Caldwell, D. O.; Dieterle, B. D., et al. The Liquid Scintillator Neutrino Detector and LAMPF Neutrino Source. Nucl. Instrum. Meth. A 1997, 388, 149–72. DOI: 10.1016/S0168-9002(96)01155-2.
- ↑ B8378 2-(4-tert-Butylphenyl)-5-(4-biphenylyl)-1,3,4-oxadiazole ≥99%; Sigma-Aldrich, <http://www.sigmaaldrich.com/catalog/ProductDetail.do?D7=0&N5=Product%20No.>. (accessed 22 May 2010).
External links
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See also the corresponding article on Wikipedia. |
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