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零场核磁共振增强的顺磁氢交换可逆性。

Zero-field NMR enhanced by parahydrogen in reversible exchange.

机构信息

Materials Science Division, Lawrence Berkeley National Laboratory, Berkeley California 94720, USA.

出版信息

J Am Chem Soc. 2012 Mar 7;134(9):3987-90. doi: 10.1021/ja2112405. Epub 2012 Feb 22.

Abstract

We have recently demonstrated that sensitive and chemically specific NMR spectra can be recorded in the absence of a magnetic field using hydrogenative parahydrogen induced polarization (PHIP) (1-3) and detection with an optical atomic magnetometer. Here, we show that non-hydrogenative parahydrogen-induced polarization (4-6) (NH-PHIP) can also dramatically enhance the sensitivity of zero-field NMR. We demonstrate the detection of pyridine, at concentrations as low as 6 mM in a sample volume of 250 μL, with sufficient sensitivity to resolve all identifying spectral features, as supported by numerical simulations. Because the NH-PHIP mechanism is nonreactive, operates in situ, and eliminates the need for a prepolarizing magnet, its combination with optical atomic magnetometry will greatly broaden the analytical capabilities of zero-field and low-field NMR.

摘要

我们最近证明,使用氢化 Para 氢诱导极化(PHIP)(1-3)和光学原子磁力计检测,可以在没有磁场的情况下记录到灵敏且具有化学特异性的 NMR 谱。在这里,我们表明非氢化 Para 氢诱导极化(4-6)(NH-PHIP)也可以极大地提高零场 NMR 的灵敏度。我们证明了在 250 μL 的样品体积中,浓度低至 6 mM 的吡啶的检测,灵敏度足以分辨所有鉴定的光谱特征,这得到了数值模拟的支持。由于 NH-PHIP 机制是非反应性的,在原位操作,并且消除了对预极化磁铁的需求,因此将其与光学原子磁力计结合使用将极大地扩展零场和低场 NMR 的分析能力。

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