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Gas‐phase transuranium chemistry: reactions of actinide ions with alcohols and thiols
Author(s) -
Gibson John K.
Publication year - 1999
Publication title -
journal of mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 1076-5174
DOI - 10.1002/(sici)1096-9888(199911)34:11<1166::aid-jms876>3.0.co;2-z
Subject(s) - chemistry , actinide , lanthanide , medicinal chemistry , bond cleavage , adduct , agostic interaction , alcohol , hydride , inorganic chemistry , ion , organic chemistry , catalysis , metal
The laser ablation with prompt reaction and detection method was employed to provide a survey of some gas‐phase reactions of actinide (M = U, Np, Pu and Am) and lanthanide (M = Tb and Tm) ions, M + and MO 1,2 + , with alcohols, thiols and ethers. Particular attention was given the changing behavior in progressing across the actinide series beyond uranium. With alcohols, ROH, major products included hydroxides and alkoxides, M(OH) 1,2 + , M(OR) 1,2 + , MO(OH) + and MO(OR) + ; these products are presumed to have resulted from ROH and ROH bond cleavage by ablated M + and MO + . The abundance distributions for these elementary products reflected the decrease in stabilities of high oxidation states between U and Am. Other alcohol reaction products included electrostatically bonded adducts, such as HONp + …C 3 H 7 OH, σ‐bonded organometallics, such as HOPu + C 2 H 5 , and π‐bonded organometallics, such as Np + η 3 ‐{C 3 H 5 }. In view of the inability of actinide and lanthanide ions to dehydrogenate alkanes, the exhibition of dehydrogenation of the alkyl chain of alcohols, as in HO–Pu + –C 3 H 5 O from propanol, suggests a non‐insertion mechanism involving complexation of the reactant ion to the alcohol. Whereas O abstraction products from ROH were obfuscated by directly ablated MO 1,2 + , S abstraction from thiols, RSH, was manifested by the appearance of MS + , MS 2 + and MOS + . In analogy with OH abstraction from alcohols to produce metal hydroxides, SH abstraction from thiols resulted in hydrosulfides, including Am(SH) + and Np(SH) 2 + . In addition to several other reaction pathways with the thiol reagents, products presumed to be thiolates included Am(C 3 H 7 S) + and NpO(C 3 H 7 S) from propanethiol. A primary product of reaction with dimethyl ether were methoxides resulting from CO bond cleavage, including Am(OCH 3 ) + and Np(OCH 3 ) 2 + . With methyl vinyl ether, more complex pathways were exhibited, most of which corresponded to the elimination of stable organic molecules. An ancillary result was the discovery of several small oxide clusters, Am 2 O n + , Np 2 O n + and AmNpO n + . The compositions and abundance distributions of these clusters reflected the propensity of Np to exist in higher oxidation states than Am; the dominant binary clusters were Am 2 O 2 + and Np 2 O 3 + . Copyright © 1999 John Wiley & Sons, Ltd.