This study utilized Matrix Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry, Thermogravimetric Analysis, Differential Scanning Calorimetry, X-Ray Diffraction, and Dielectric Analysis to assess the viscoelastic and structural properties of three generations of tert-butyl and meth
Ester- and amide-terminated dendrimers with alternating amide and ether generations
✍ Scribed by Yijun Pan; Warren T. Ford
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 188 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0887-624X
No coin nor oath required. For personal study only.
✦ Synopsis
Ester-terminated polyamide dendrimers up to the third generation and amide-terminated polyamide dendrimers of the first generation were synthesized by convergent growth. The Williamson ether synthesis and diphenylphosphoryl azide (DPPA) coupling of amines to carboxylic acids were used for the construction of the dendrimers, having alternate ether and amide generations. The methyl ester-and N,N-diethylamide-terminated dendrimers were readily soluble in common organic solvents while the N-methylamide-and N-benzylamide-terminated dendrimers were soluble only in DMF and DMSO. Both the end and internal amide groups of the N,Ndiethylamide-terminated dendrimer were reduced by LiAlH 4 to form a polyamine dendrimer.
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