Literature DB >> 26744294

Contact Ion Pairs on a Protonated Azamacrocycle: the Role of the Anion Basicity.

Caterina Fraschetti1, Antonello Filippi1, Maria Elisa Crestoni1, Enrico Marcantoni2, Marco Glucini2, Laura Guarcini1, Maria Montagna1, Leonardo Guidoni3, Maurizio Speranza4.   

Abstract

A potassium-containing hexaazamacrocyclic dication, [M•H•K](2+), is able to add in the gas phase mono- and dicarboxylate anions as well as inorganic anions by forming the corresponding monocharged adducts, the structure of which markedly depends on the basicity of the anion. With anions, such as acetate or fluoride, the neutral hexaazamacrocycle M acts as an acceptor of monosolvated K(+) ion. With less basic anions, such as trifluoroacetate or chloride, the protonated hexaazamacrocycle [M•H](+) performs the unusual functions of an acceptor of contact K(+)/anion pairs. Graphical Abstract ᅟ.

Entities:  

Keywords:  Ab initio molecular dynamics; Azamacrocycles; Contact ion pairs; ESI-MS; Ion–ion reactions

Mesh:

Substances:

Year:  2016        PMID: 26744294     DOI: 10.1007/s13361-015-1327-3

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  21 in total

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  1 in total

Review 1.  Imine- and Amine-Type Macrocycles Derived from Chiral Diamines and Aromatic Dialdehydes.

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  1 in total

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