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Terminal Diazirines Enable Reverse Polarization Transfer from 15 N2 Singlets.
Zhang, Guannan; Colell, Johannes F P; Glachet, Thomas; Lindale, Jacob R; Reboul, Vincent; Theis, Thomas; Warren, Warren S.
Afiliación
  • Zhang G; Department of Chemistry, Duke University, Durham, NC, 27708, USA.
  • Colell JFP; Department of Chemistry, Duke University, Durham, NC, 27708, USA.
  • Glachet T; Normandie Univ, LCMT, ENSICAEN, UNICAEN, CNRS, 14000, Caen, France.
  • Lindale JR; Department of Chemistry, Duke University, Durham, NC, 27708, USA.
  • Reboul V; Normandie Univ, LCMT, ENSICAEN, UNICAEN, CNRS, 14000, Caen, France.
  • Theis T; Department of Chemistry, NC State University, Raleigh, NC, 27695, USA.
  • Warren WS; Department of Chemistry, Duke University, Durham, NC, 27708, USA.
Angew Chem Int Ed Engl ; 58(32): 11118-11124, 2019 08 05.
Article en En | MEDLINE | ID: mdl-31168901
Diazirine moieties are chemically stable and have been incorporated into biomolecules without impediment of biological activity. The 15 N2 labeled diazirines are appealing motifs for hyperpolarization supporting relaxation protected states with long-lived lifetimes. The (-CH15 N2 ) diazirine groups investigated here are analogues to methyl groups, which provides the opportunity to transfer polarization stored on a relaxation protected (-CH15 N2 ) moiety to 1 H, thus combining the advantages of long lifetimes of 15 N polarization with superior sensitivity of 1 H detection. Despite the proximity of 1 H to 15 N nuclei in the diazirine moiety, 15 N T1 times of up to (4.6±0.4) min and singlet lifetimes Ts of up to (17.5±3.8) min are observed. Furthermore, we found terminal diazirines to support hyperpolarized 1 H2 singlet states in CH2 groups of chiral molecules. The singlet lifetime of 1 H singlets is up to (9.2±1.8) min, thus exceeding 1 H T1 relaxation time (at 8.45 T) by a factor of ≈100.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Azirinas Idioma: En Revista: Angew Chem Int Ed Engl Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Azirinas Idioma: En Revista: Angew Chem Int Ed Engl Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos