Widjaja Effendi, Tan Wei Jian
Institute of Chemical and Engineering Sciences, Jurong Island Singapore.
Appl Spectrosc. 2008 Aug;62(8):889-94. doi: 10.1366/000370208785284286.
The solid-state intramolecular cyclization of lisinopril to diketopiperazine was investigated by in situ Fourier transform infrared (FT-IR) microscopy. Using a controllable heating cell, the isothermal transformation was monitored in situ at 147.5, 150, 152.5, 155, and 157.5 degrees C. The collected time-dependent FT-IR spectra at each isothermal temperature were preprocessed and analyzed using a multivariate chemometric approach. The pure component spectra of the observable component (lisinopril and diketopiperazine) were resolved and their time-dependent relative contributions were also determined. Model-free and various model fitting methods were implemented in the kinetic analysis to estimate the activation energy of the intramolecular cyclization reaction. Arrhenius plots indicate that the activation energy is circa 327 kJ/mol.
通过原位傅里叶变换红外(FT-IR)显微镜研究了赖诺普利向二酮哌嗪的固态分子内环化反应。使用可控加热池,在147.5、150、152.5、155和157.5摄氏度下原位监测等温转变。对每个等温温度下收集的随时间变化的FT-IR光谱进行预处理,并使用多元化学计量学方法进行分析。解析了可观察组分(赖诺普利和二酮哌嗪)的纯组分光谱,并确定了它们随时间变化的相对贡献。在动力学分析中采用了无模型和各种模型拟合方法来估计分子内环化反应的活化能。阿累尼乌斯图表明活化能约为327 kJ/mol。