
Organic Mass Spectrometry p. 342 - 349 (1988)
Update date:2022-07-29
Topics:
Kiplinger, Jeffrey P.
Bursey, Maurice M.
The utility of the collisional activation technique in structure determination of ions is limited as parent ion mass increases.Optimum cillisionally activated dissociation yield is often obtained at parent masses of 1000-2000 u, after which daughter ion yield decreases.The apparent decrease in the efficiency of the collisional activation process has been thought of as a degree-of-freedom effect: as new rotational-vibrational modes are added to the parent ion, its lifetime with respect to dissociation increases.We have investigated this effect using an easily characterized system of several poly(ethylene glycol) homologs from the 15-mer to the 35-mer.Observed trends in the collisional activation spectra as parent mass increases support the postulated 'degree-of-freedom' effect in general.The loss of C2H4O from the a fragmentation which has a high activation barrier, however, actually becomes more favored as the parent ion becomes larger.This effect is explained in terms of statistical rate theory.
Dalian Join King Biochemical Tech. Co., Ltd.
Contact:0411 39216206
Address:814 First State Blvd
Shandong General Materials Co.,Ltd(Shandong Aoertong Chemical Co., Ltd)
Contact:86-531-88072280
Address:No. 1825 Hualong Road, Licheng District, Jinan, Shandong, China
Nanjing Spring & Autumn Biological Engineering Co., Ltd.
Contact:86-180510-83338
Address:Suite# 210, No. 1 BuildingNanjing Agricultural Biotechnology High-tech Entrepreneurship Center, No. 4 Tongwei Road, Xuanwu District, Nanjing,China
Guangxi Shanyun Biochemical Science and Technology Co., Ltd
Contact:+86-0772--6828887
Address:#2 Industrial Park of Luzhai County, Liuzhou, Guangxi, China
Guangzhou Flower's Song Fine Chemical CO,. Ltd
Contact:+86-20-87475199
Address:No.12, Fenghuang 3 Road, Jiulong Industrial Park, Luogang District, Guangzhou. China
Doi:10.1016/S0022-328X(01)01359-6
(2002)Doi:10.1021/acs.jmedchem.9b01194
(2019)Doi:10.1016/j.tet.2006.06.058
(2006)Doi:10.1039/b201147f
(2002)Doi:10.1039/d0ob00811g
(2020)Doi:10.1039/c7cc02088k
(2017)