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Using signal amplification by reversible exchange (SABRE) to hyperpolarise 119Sn and 29Si NMR nuclei.


ABSTRACT: The hyperpolarisation of the 119Sn and 29Si nuclei in 5-(tributylstannyl)pyrimidine (ASn) and 5-(trimethylsilyl)pyrimidine (BSi) is achieved through their reaction with [IrCl(COD)(IMes)] (1a) or [IrCl(COD)(SIMes)] (1b) and parahydrogen via the SABRE process. 1a exhibits superior activity in both cases. The two inequivalent pyrimidine proton environments of ASn readily yielded signal enhancements totalling ?2300-fold in its 1H NMR spectrum at a field strength of 9.4 T, with the corresponding 119Sn signal being 700 times stronger than normal. In contrast, BSi produced analogous 1H signal gains of ?2400-fold and a 29Si signal that could be detected with a signal to noise ratio of 200 in a single scan. These sensitivity improvements allow NMR detection within seconds using micromole amounts of substrate and illustrate the analytical potential of this approach for high-sensitivity screening. Furthermore, after extended reaction times, a series of novel iridium trimers of general form [Ir(H)2Cl(NHC)(?-pyrimidine-?N:?N')]3 precipitate from these solutions whose identity was confirmed crystallographically for BSi.

SUBMITTER: Olaru AM 

PROVIDER: S-EPMC5436037 | biostudies-literature | 2016 Dec

REPOSITORIES: biostudies-literature

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Using signal amplification by reversible exchange (SABRE) to hyperpolarise <sup>119</sup>Sn and <sup>29</sup>Si NMR nuclei.

Olaru Alexandra M AM   Burt Alister A   Rayner Peter J PJ   Hart Sam J SJ   Whitwood Adrian C AC   Green Gary G R GGR   Duckett Simon B SB  

Chemical communications (Cambridge, England) 20161201 100


The hyperpolarisation of the <sup>119</sup>Sn and <sup>29</sup>Si nuclei in 5-(tributylstannyl)pyrimidine (A<sub>Sn</sub>) and 5-(trimethylsilyl)pyrimidine (B<sub>Si</sub>) is achieved through their reaction with [IrCl(COD)(IMes)] (1a) or [IrCl(COD)(SIMes)] (1b) and parahydrogen via the SABRE process. 1a exhibits superior activity in both cases. The two inequivalent pyrimidine proton environments of A<sub>Sn</sub> readily yielded signal enhancements totalling ∼2300-fold in its <sup>1</sup>H NMR  ...[more]

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