𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Cold-spray ionization mass spectrometry: principle and applications

✍ Scribed by Kentaro Yamaguchi


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
678 KB
Volume
38
Category
Article
ISSN
1076-5174

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

A direct solution analysis method, cold‐spray ionization (CSI) mass spectrometry (MS), a variant of electrospray (ESI) MS operating at low temperature (ca −80 to 10 °C), allows the facile and precise characterization of labile organic species, especially those in which non‐covalent bonding interactions are prominent. We applied this method to investigations of the solution structures of many labile organic species, including unstable reagents and reaction intermediates, asymmetric catalysts, supramolecules and even primary biomolecules. Remarkable analytical results were obtained for highly ordered supramolecules using the CSI method. Whereas conventional ESI is not applicable to these compounds because of their instability to heat and/or air, CSI affords multiply charged molecular ions with many solvent molecules attached. Investigation of the constitution of Grignard reagents in solution is extremely challenging, but CSI‐MS allowed us to identify one of the key structures in THF solution. Recently, this method was adopted for investigations of the solution structures of primary biomolecules such as nucleosides, amino acids, sugars and lipids, revealing singly charged Na^+^ adducts of large clusters (chain structures), presumably linked by non‐covalent interactions, including hydrogen bonding and/or hydrophobic interactions. The principle of the CSI method and applications of the method to a wide variety of labile organic species and primary biomolecules in solution are described. Copyright © 2003 John Wiley & Sons, Ltd.


📜 SIMILAR VOLUMES


Hyperstranded DNA Architectures Observed
✍ Shigeru Sakamoto; Kentaro Yamaguchi 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 803 KB

washing manipulations in the entire array. Significantly, the efficiency of the synthesis does not depend on the number of building blocks used along each axis. This feature provides a unique advantage of this method over the use of 2D arrays, representing a direct alternative to the split synthesis