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Volumn 323, Issue 5922, 2009, Pages 1711-1714

Increasing hyperpolarized spin lifetimes through true singlet eigenstates

Author keywords

[No Author keywords available]

Indexed keywords

2,3 BUTANEDIONE; 2,3 CARBON 13 LABELED DIACETYL; UNCLASSIFIED DRUG;

EID: 63449130233     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1167693     Document Type: Article
Times cited : (184)

References (31)
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    • D. A. Hall et al., Science 276, 930 (1997).
    • (1997) Science , vol.276 , pp. 930
    • Hall, D.A.1
  • 9
    • 33845292936 scopus 로고    scopus 로고
    • K. Golman et al., Cancer Res. 66, 10855 (2006).
    • (2006) Cancer Res , vol.66 , pp. 10855
    • Golman, K.1
  • 14
    • 63449130468 scopus 로고    scopus 로고
    • The nomenclature used here is explained more fully, with specific examples, in textbooks such as 15
    • The nomenclature used here is explained more fully, with specific examples, in textbooks such as (15).
  • 20
    • 63449124076 scopus 로고    scopus 로고
    • See http://seattlepi.nwsource.com/dayart/20071221/ DiacetylProducts2.pdf for a study done by the Seattle Post-Intelligencer in December 2007.
    • See http://seattlepi.nwsource.com/dayart/20071221/ DiacetylProducts2.pdf for a study done by the Seattle Post-Intelligencer in December 2007.
  • 22
    • 10044289888 scopus 로고
    • and references therein
    • R. P. Bell, Adv. Phys. Org. Chem. 4, 1 (1966) and references therein.
    • (1966) Adv. Phys. Org. Chem , vol.4 , pp. 1
    • Bell, R.P.1
  • 31
    • 63449132739 scopus 로고    scopus 로고
    • This work was supported by the NIH under grant EB02122 and by the North Carolina Biotechnology Center. We thank D. Bhattacharyya for his help in determining optimal conditions to hyperpolarize diacetyl; M. Jenista for help with calculations; T. Ribiero for his assistance in running NMR spectra; L. Bouchard for discussions of singlet character in strongly coupled systems; and S. Craig, E. Toone, D. Coltart, and M. S. Warren for particularly useful discussions on the chemistry of these compounds. A provisional patent has been submitted on this work by W.S.W. and Duke University
    • This work was supported by the NIH under grant EB02122 and by the North Carolina Biotechnology Center. We thank D. Bhattacharyya for his help in determining optimal conditions to hyperpolarize diacetyl; M. Jenista for help with calculations; T. Ribiero for his assistance in running NMR spectra; L. Bouchard for discussions of singlet character in strongly coupled systems; and S. Craig, E. Toone, D. Coltart, and M. S. Warren for particularly useful discussions on the chemistry of these compounds. A provisional patent has been submitted on this work by W.S.W. and Duke University.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.