Scalable synthesis of sequence-defined, unimolecular macromolecules by Flow-IEG

被引:150
作者
Leibfarth, Frank A. [1 ]
Johnson, Jeremiah A. [1 ]
Jamison, Timothy F. [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
polymers; automation; continuous flow chemistry; unimolecular macromolecules; sequence-controlled polymers; CONTROLLED POLYMERS; CLICK-CHEMISTRY; OLIGOMERS; DNA; POLYMERIZATION; MACROCYCLES; TECHNOLOGY; ACIDS;
D O I
10.1073/pnas.1508599112
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We report a semiautomated synthesis of sequence and architecturally defined, unimolecular macromolecules through a marriage of multistep flow synthesis and iterative exponential growth (Flow-IEG). The Flow-IEG system performs three reactions and an in-line purification in a total residence time of under 10 min, effectively doubling the molecular weight of an oligomeric species in an uninterrupted reaction sequence. Further iterations using the Flow-IEG system enable an exponential increase in molecular weight. Incorporating a variety of monomer structures and branching units provides control over polymer sequence and architecture. The synthesis of a uniform macromolecule with a molecular weight of 4,023 g/mol is demonstrated. The user-friendly nature, scalability, and modularity of Flow-IEG provide a general strategy for the automated synthesis of sequence-defined, unimolecular macromolecules. Flow-IEG is thus an enabling tool for theory validation, structure-property studies, and advanced applications in biotechnology and materials science.
引用
收藏
页码:10617 / 10622
页数:6
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