Laskin J, Lifshitz C
Pacific Northwest National Laboratory, William R. Wiley Environmental Molecular Science Laboratory, P.O. Box 999 (K8-96), Richland, Washington 99352, USA.
J Mass Spectrom. 2001 May;36(5):459-78. doi: 10.1002/jms.164.
Kinetic energy releases (KERs) in unimolecular fragmentations of singly and multiply charged ions provide information concerning ion structures, reaction energetics and dynamics. This topic is reviewed covering both early and more recent developments. The subtopics discussed are as follows: (1) introduction and historical background; (2) ion dissociation and kinetic energy release: kinematics; potential energy surfaces; (3) the kinetic energy release distribution (KERD); (4) metastable peak observations: measurements on magnetic sector and time-of-flight instruments; energy selected results by photoelectron photoion coincidence (PEPICO); (5) extracting KERDs from metastable peak shapes; (6) ion structure determination and reaction mechanisms: singly and multiply charged ions; biomolecules and fullerenes; (7) theoretical approaches: phase space theory (PST), orbiting transition state (OTS)/PST, finite heat bath theory (FHBT) and the maximum entropy method; (8) exit channel interactions; (9) general trends: time and energy dependences; (10) thermochemistry: organometallic reactions, proton-bound clusters, fullerenes; and (11) the efficiency of phase space sampling.
单电荷和多电荷离子单分子碎裂过程中的动能释放(KERs)提供了有关离子结构、反应能量学和动力学的信息。本文对这一主题进行了综述,涵盖了早期和近期的发展。讨论的子主题如下:(1)引言和历史背景;(2)离子解离和动能释放:运动学;势能面;(3)动能释放分布(KERD);(4)亚稳峰观测:在磁扇形和飞行时间仪器上的测量;光电子光离子符合(PEPICO)的能量选择结果;(5)从亚稳峰形状中提取KERD;(6)离子结构测定和反应机理:单电荷和多电荷离子;生物分子和富勒烯;(7)理论方法:相空间理论(PST)、轨道过渡态(OTS)/PST、有限热浴理论(FHBT)和最大熵方法;(8)出射通道相互作用;(9)一般趋势:时间和能量依赖性;(10)热化学:有机金属反应、质子结合簇、富勒烯;以及(11)相空间采样效率。