Bayat Parisa, Gatineau David, Lesage Denis, Marhabaie Sina, Martinez Alexandre, Cole Richard B
Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, IPCM, 75252, Paris, France.
Univ. Grenoble Alpes and CNRS, DCM (UMR 5250) BP 53, 38041, Grenoble Cedex 9, France.
J Mass Spectrom. 2019 May;54(5):437-448. doi: 10.1002/jms.4345.
A low-energy collision induced dissociation (CID) (low-energy CID) approach that can determine both activation energy and activation entropy has been used to evaluate gas-phase binding energies of host-guest (H-G) complexes of a heteroditopic hemicryptophane cage host (Zn (II)@1) with a series of biologically relevant guests. In order to use this approach, preliminary calibration of the effective temperature of ions undergoing resonance excitation is required. This was accomplished by employing blackbody infrared radiative dissociation (BIRD) which allows direct measurement of activation parameters. Activation energies and pre-exponential factors were evaluated for more than 10 H-G complexes via the use of low-energy CID. The relatively long residence time of the ions inside the linear ion trap (maximum of 60 s) allowed the study of dissociations with rates below 1 s . This possibility, along with the large size of the investigated ions, ensures the fulfilment of rapid energy exchange (REX) conditions and, as a consequence, accurate application of the Arrhenius equation. Compared with the BIRD technique, low-energy CID allows access to higher effective temperatures, thereby permitting one to probe more endothermic decomposition pathways. Based on the measured activation parameters, guests bearing a phosphate (-OPO ) functional group were found to bind more strongly with the encapsulating cage than those having a sulfonate (-SO ) group; however, the latter ones make stronger bonds than those with a carboxylate (-CO ) group. In addition, it was observed that the presence of trimethylammonium (-N(CH ) ) or phenyl groups in the guest's structure improves the strength of H-G interactions. The use of this technique is very straightforward, and it does not require any instrumental modifications. Thus, it can be applied to other H-G chemistry studies where comparison of bond dissociation energies is of paramount importance.
一种能够同时测定活化能和活化熵的低能碰撞诱导解离(CID)(低能CID)方法,已被用于评估一种异二位点半穴醚笼状主体(Zn (II)@1)与一系列具有生物学相关性的客体形成的主客体(H-G)配合物的气相结合能。为了使用这种方法,需要对经历共振激发的离子的有效温度进行初步校准。这是通过采用黑体红外辐射解离(BIRD)来实现的,该方法允许直接测量活化参数。通过使用低能CID,对10多种H-G配合物的活化能和指前因子进行了评估。离子在线性离子阱内相对较长的停留时间(最长60秒)使得能够研究解离速率低于1秒的解离过程。这种可能性,连同所研究离子的大尺寸,确保了快速能量交换(REX)条件的满足,因此能够准确应用阿伦尼乌斯方程。与BIRD技术相比,低能CID能够达到更高的有效温度,从而使人们能够探测更多吸热的分解途径。基于所测量的活化参数,发现带有磷酸根(-OPO )官能团的客体与包封笼的结合比带有磺酸根(-SO )基团的客体更强;然而,后者形成的键比带有羧酸根(-CO )基团的客体更强。此外,观察到客体结构中存在三甲基铵(-N(CH ) )或苯基会提高H-G相互作用的强度。该技术的使用非常简单,并且不需要对仪器进行任何修改。因此,它可以应用于其他对键解离能比较至关重要的H-G化学研究中。