Alkali-hydrolysis of D-glucono-delta-lactone studied by chiral Raman and circular dichroism spectroscopies  

Alkali-hydrolysis of D-glucono-delta-lactone studied by chiral Raman and circular dichroism spectroscopies

在线阅读下载全文

作  者:JIA GuoQing QIU Shi LI GuanNa ZHOU Jun FENG ZhaoChi LI Can 

机构地区:[1]State Key Laboratory of Catalysis,Dalian Institute of Chemical Physics,Chinese Academy of Sciences,Dalian 116023,China [2]Graduate University of Chinese Academy of Sciences,Beijing 100049,China

出  处:《Science China Chemistry》2009年第5期552-558,共7页中国科学(化学英文版)

基  金:Supported by the National Natural Science Foundation of China (Grant Nos. 20621063, 20773123, and 20673110);Programme for Strategic Scientific Alli-ances between China and the Netherlands (Grant No. 2008DFB50130)

摘  要:The alkali-hydrolysis of D-glucono-delta-lactone (GDL) was investigated by chiral Raman and circular dichroism (CD) spectroscopies in combination with density functional theory calculation. Based on the characteristic CD bands of GDL and its hydrolysis product, the dynamics of hydrolysis was studied using stopped-flow CD method. Using chiral Raman spectroscopy (CRS), the stereochemical change of GDL owing to the hydrolysis reaction was discussed on the vibrational scale. The CRS results show that the ring-opening due to hydrolysis has a great influence on the chiral structure around the car-bonyl group, which was evidenced by the disappearance of the CRS band at 1735 cm-1 (C== O stretching vibrational mode). In addition, the change of positions and intensity of CRS bands was also observed, which was ascribed to the perturbation around the C2, C3, C4 and C5 carbons due to ring-opening. It is worthy to note that the stereochemistry of C2, C3, C4 and C5 had no fundamental change during the hydrolysis reaction, which was reflected in the maintenance of the signs of the CRS bands. Our results demonstrate that in comparison with CD technique, CRS may provide more detailed structural information of chiral molecules and open up new vistas of research for chiral reactions.The alkali-hydrolysis of D-glucono-delta-lactone (GDL) was investigated by chiral Raman and circular dichroism (CD) spectroscopies in combination with density functional theory calculation. Based on the characteristic CD bands of GDL and its hydrolysis product, the dynamics of hydrolysis was studied using stopped-flow CD method. Using chiral Raman spectroscopy (CRS), the stereochemical change of GDL owing to the hydrolysis reaction was discussed on the vibrational scale. The CRS results show that the ring-opening due to hydrolysis has a great influence on the chiral structure around the carbonyl group, which was evidenced by the disappearance of the CRS band at 1735 cm 1 (C=O stretching vibrational mode). In addition, the change of positions and intensity of CRS bands was also observed, which was ascribed to the perturbation around the C2, C3, C4 and C5 carbons due to ring-opening. It is worthy to note that the stereochemistry of C2, C3, C4 and C5 had no fundamental change during the hydrolysis reaction, which was reflected in the maintenance of the signs of the CRS bands. Our results demonstrate that in comparison with CD technique, CRS may provide more detailed structural information of chiral molecules and open up new vistas of research for chiral reactions.

关 键 词:CHIRAL RAMAN spectroscopy (CRS) circular dichroism (CD) STOPPED-FLOW D-glucono-delta-lactone (GDL) HYDROLYSIS 

分 类 号:O657.3[理学—分析化学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象