Living crystallization-driven self-assembly(CDSA)provides robust access to uniformπ-conjugated nanostructures(CNSs)from block copolymers(BCPs)containing a crystallineπ-conjugated segment with controlled dimension,mo...Living crystallization-driven self-assembly(CDSA)provides robust access to uniformπ-conjugated nanostructures(CNSs)from block copolymers(BCPs)containing a crystallineπ-conjugated segment with controlled dimension,morphology and composition,which show appealing applications in biomedicine,photocatalysis and microelectronics.To further expand the application spectrum of these CNSs,the development of facile strategies toward diverse CNSs with varying structures/functionalities is highly desired.Herein,BCPs consisting of oligo(p-phenylene ethynylene)-b-poly(polypropyl-3-methanethiol acrylate)(OPE_(9)-bPMTPA35and OPE_(9)-b-PMTPA_(58);the subscript represents the number of repeat unit of each block)consisting of a crystallineπ-conjugated core-forming OPE_(9)segment and a corona-forming PMTPA block are synthesized.By efficient“click-type”alkylation of methylthio groups,OPE_(9)-b-PMTPA with varying contents of sulfonium unit is obtained.Uniform ribbon-like micelles with different widths and lengths can then be generated in a controlled manner via the self-seeding approach of living CDSA.Additionally,negatively charged polymeric and Ag nanoparticles can be immobilized on sulfonium/methylthio-containing shells by taking advantage of electrostatic attraction and coordination interaction,respectively.Interestingly,the ribbon-like micelles with positively charged shells exhibit antibacterial activity against E.coli.Given the ease of modification of PMTPA-based shell and attractive opto-electronic/photocatalytic properties ofπ-conjugated units,the combination of methylthio-chemistry and living CDSA opens a new avenue to generate multi-functional CNSs for widespread applications from biomedicine to photocatalysis.展开更多
The structure of side chains ofπ-conjugated segments is a critical factor determining living crystallization-driven self-assembly(CDSA),a versatile platform to generate fiber-like nanostructures with precise length a...The structure of side chains ofπ-conjugated segments is a critical factor determining living crystallization-driven self-assembly(CDSA),a versatile platform to generate fiber-like nanostructures with precise length and composition.Herein,we design and synthesize three block copolymers(BCPs)containing same corona-forming poly(N-isopropyl acrylamide)(PNIPAM)segment,but different core-formingπ-conjugated oligo(p-phenylene vinylene)(OPV)with linear pentyl(l-OPV),racemic 2-methyl butyl(r-OPV)and stereo-regular chiral(S)-2-methyl butyl(c-OPV)side chains,respectively.By using these BCPs of l-OPV-b-PNIPAM_(47),r-OPV-b-PNIPAM_(47)and c-OPV-b-PNIPAM_(47)as model,we aim to get a deep insight into how steric and stereo-regular effect induced by branched alkyl side chains of OPV segment affects the living CDSA.The results showed that l-OPV-b-PNIPAM_(47)exhibits typical characteristics of self-seeding and seeded growth of living CDSA to give uniform fiber-like micelles of controlled length.On the contrary,r-OPV-b-PNIPAM_(47)and c-OPV-b-PNIPAM_(47)with branched racemic and stereo-regular chiral alkyl side chains are more prone to self-nucleation during the micellar elongation to give short and polydisperse fiber-like micelles.The obvious selfnucleation during the micellar elongation of r-OPV-b-PNIPAM_(47)and c-OPV-b-PNIPAM_(47)is due to the increase of steric repulsion with OPV units induced by branched alkyl side chains,not the stereo-irregular effect of racemic alkyl side chains.展开更多
The self-assembly of five narrowly distributed novel rod-coil diblock copolymers, poly(styrene-block-(2, 5-bis[4-methoxy-phenyl]oxycarbonyl) styrene) (PS-b-PMPCS), in p-xylene, a selective solvent at room temperature,...The self-assembly of five narrowly distributed novel rod-coil diblock copolymers, poly(styrene-block-(2, 5-bis[4-methoxy-phenyl]oxycarbonyl) styrene) (PS-b-PMPCS), in p-xylene, a selective solvent at room temperature, was studied. Therod-coil copolymers, which have the same PS length but different PMPCS length, were synthesized by 2,2,6,6-tetramethyl-I-piperidinyloxy (TEMPO) mediated living free radical polymerization. The influence of the rod length on the self-assemblymorphology was studied by transmission electron microscopy (TEM). At a concentration of 2.0 mg/mL, those copolymerswith relatively shorter PMPCS length (copolymers 1 and 2) form individual spherical micelles; those with relatively longerPMPCS length (copolymer 3 and 4) form 'pearl chains' coexisting with individual spherical micelles; the ones with longestPMPCS length form 'pearl chains' coexisting with occasionally formed nanofibers. The diameter of all the morphologieswas controlled by the rod length. This gives us a way to govern the self-assembly morphology by altering the length of oneblock in the block copolymer.展开更多
Herein we demonstrate crystallization-driven self-assembly ofisotactic polystyrene (iPS) with high isotacticity and narrow molecular weight distribution and crystallization-induced switching of the morphology of iPS...Herein we demonstrate crystallization-driven self-assembly ofisotactic polystyrene (iPS) with high isotacticity and narrow molecular weight distribution and crystallization-induced switching of the morphology of iPS aggregates in N, N-dimethylformamide (DMF). The formation and morphology switching of the self-assembled aggregates of iPS are investigated by means of dynamic light scattering (DLS), scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and wide angle X-ray diffraction (WXRD). The results reveal that cooling DMF solution of iPS promotes iPS chains to self-assemble into spherical aggregates with a gelled core cross-linked by microcrystals, which is surrounded by solvent-swollen corona. Furthermore, crystallization induces the deformation of iPS aggregates from spherical to plate-like or nest-like.展开更多
Fragmentation/disassembly of fiber-like micelles generated by living crystalline-driven self-assembly(CDSA)is usually encountered in aqueous media,which hinders the applications of micelles.Herein,we report the genera...Fragmentation/disassembly of fiber-like micelles generated by living crystalline-driven self-assembly(CDSA)is usually encountered in aqueous media,which hinders the applications of micelles.Herein,we report the generation of uniform fiber-like micelles consisting of a𝜋Л-conjugated oligo(p-phenylenevinylene)core and a crosslinking silica shell with grafted poly(ethylene glycol)(PEG)chains by the combination of living CDSA,silica chemistry and surface grafting-onto strategy.Owing to the presence of crosslinking silica shell and the outmost PEG chains,the resulting micelles exhibit excellent dispersity and colloidal stability in PBS buffer,BSA aqueous solution and upon heating at 80℃ for 2 h without micellar fragmentation/disassembly.The micelles also show negligible cytotoxicity toward both HeLa cervical cancer and HEK239T human embryonic kidney cell lines.Interestingly,micelles with Ln of 156 nm show the“stealth”property with no significant uptake by HeLa cells,whereas some certain amounts of micelles with Ln of 535 nm can penetrate into HeLa cells,showing length-dependent cellular uptake behaviors.These results provide a route to prepare uniform,colloidally stable fiber-like nanostructures with tunable length and functions derived for biomedical applications.展开更多
Supramolecular polymerization properties have been studied for a series of perylene bisimide(PBI)dyes containing identical hydrogen-bonding amide groups in imide positions but variable number or size of alkoxy substit...Supramolecular polymerization properties have been studied for a series of perylene bisimide(PBI)dyes containing identical hydrogen-bonding amide groups in imide positions but variable number or size of alkoxy substituents in bay-positions.展开更多
Information-rich molecules provide opportunities for evolution.Genetically engineered materials are superior in that their properties are coded within genetic sequences and could be fine-tuned.In this review,we elabor...Information-rich molecules provide opportunities for evolution.Genetically engineered materials are superior in that their properties are coded within genetic sequences and could be fine-tuned.In this review,we elaborate the concept of genetically engineered materials(GEMs)using examples ranging from engineered protein materials to engineered living materials.Proteinbased materials are the materials of choice by nature.Recent progress in protein engineering has led to opportunities to tune their sequences for optimal material performance.Proteins also play a central role in living materials where they act in concert with other biological components as well as nonbiological cofactors,giving rise to living features.While the existing GEMs are often limited to those constructed by building blocks of biological origin,being genetically engineerable does not preclude nonbiologic or synthetic materials,the latter of which have yet to be fully explored.展开更多
Block copolymers have aroused much interest,and their application has been rapidly expanded.In recent years,our group has committed to exploring synthesis and self-assembly of block copolymers.We have designed and syn...Block copolymers have aroused much interest,and their application has been rapidly expanded.In recent years,our group has committed to exploring synthesis and self-assembly of block copolymers.We have designed and synthesized several new thermo-responsive polymers and photo-responsive polymers by living/controlled radical polymerization(LCRP)and investigated their stimuli-responsive properties.Aiming at convenient and efficient synthesis of block copolymer nano-assemblies,we have developed several methods based on polymerization-induced self-assembly(PISA).Herein,we give a short summary of our research in these years.The aim of this account is to stimulate innovative synthesis strategies of block copolymer nano-assemblies,and promote more scientific research cooperation to face the exciting opportunities and challenges encountered in block copolymers.展开更多
基金supported by the National Natural Science Foundation of China(52122314,U22A20131,52273008,52361165657)the Strategic Priority Research Program of Chinese Academy of Sciences(XDB0590000)+1 种基金the Shanghai Scientific and Technological Innovation Project(21520780100,21ZR1481700,22ZR1479300,22JC1401000,22ZR1475400)the Shanghai Rising-Star Program(23QA1402500)。
文摘Living crystallization-driven self-assembly(CDSA)provides robust access to uniformπ-conjugated nanostructures(CNSs)from block copolymers(BCPs)containing a crystallineπ-conjugated segment with controlled dimension,morphology and composition,which show appealing applications in biomedicine,photocatalysis and microelectronics.To further expand the application spectrum of these CNSs,the development of facile strategies toward diverse CNSs with varying structures/functionalities is highly desired.Herein,BCPs consisting of oligo(p-phenylene ethynylene)-b-poly(polypropyl-3-methanethiol acrylate)(OPE_(9)-bPMTPA35and OPE_(9)-b-PMTPA_(58);the subscript represents the number of repeat unit of each block)consisting of a crystallineπ-conjugated core-forming OPE_(9)segment and a corona-forming PMTPA block are synthesized.By efficient“click-type”alkylation of methylthio groups,OPE_(9)-b-PMTPA with varying contents of sulfonium unit is obtained.Uniform ribbon-like micelles with different widths and lengths can then be generated in a controlled manner via the self-seeding approach of living CDSA.Additionally,negatively charged polymeric and Ag nanoparticles can be immobilized on sulfonium/methylthio-containing shells by taking advantage of electrostatic attraction and coordination interaction,respectively.Interestingly,the ribbon-like micelles with positively charged shells exhibit antibacterial activity against E.coli.Given the ease of modification of PMTPA-based shell and attractive opto-electronic/photocatalytic properties ofπ-conjugated units,the combination of methylthio-chemistry and living CDSA opens a new avenue to generate multi-functional CNSs for widespread applications from biomedicine to photocatalysis.
基金National Science Foundation for Distinguished Young Scholars(No.51825304)the National Natural Science Foundation of China(Nos.52122314,U22A20131,51873229 and 51961145103)+3 种基金the Youth Innovation Promotion Association of CAS(No.Y2020062)Shanghai Scientific and Technological Innovation Project(Nos.20JC1415400,21520780100,22JC1401000 and 22ZR1475400)Innovation Program of Shanghai Municipal Education Commission(No.2019-01-07-00-05-E00012)East China University of Science and Technology(No.SLD13223004).
文摘The structure of side chains ofπ-conjugated segments is a critical factor determining living crystallization-driven self-assembly(CDSA),a versatile platform to generate fiber-like nanostructures with precise length and composition.Herein,we design and synthesize three block copolymers(BCPs)containing same corona-forming poly(N-isopropyl acrylamide)(PNIPAM)segment,but different core-formingπ-conjugated oligo(p-phenylene vinylene)(OPV)with linear pentyl(l-OPV),racemic 2-methyl butyl(r-OPV)and stereo-regular chiral(S)-2-methyl butyl(c-OPV)side chains,respectively.By using these BCPs of l-OPV-b-PNIPAM_(47),r-OPV-b-PNIPAM_(47)and c-OPV-b-PNIPAM_(47)as model,we aim to get a deep insight into how steric and stereo-regular effect induced by branched alkyl side chains of OPV segment affects the living CDSA.The results showed that l-OPV-b-PNIPAM_(47)exhibits typical characteristics of self-seeding and seeded growth of living CDSA to give uniform fiber-like micelles of controlled length.On the contrary,r-OPV-b-PNIPAM_(47)and c-OPV-b-PNIPAM_(47)with branched racemic and stereo-regular chiral alkyl side chains are more prone to self-nucleation during the micellar elongation to give short and polydisperse fiber-like micelles.The obvious selfnucleation during the micellar elongation of r-OPV-b-PNIPAM_(47)and c-OPV-b-PNIPAM_(47)is due to the increase of steric repulsion with OPV units induced by branched alkyl side chains,not the stereo-irregular effect of racemic alkyl side chains.
基金The financial support of the National Natural Science Foundation of China (Grants. 29992590-4 and 20134010)
文摘The self-assembly of five narrowly distributed novel rod-coil diblock copolymers, poly(styrene-block-(2, 5-bis[4-methoxy-phenyl]oxycarbonyl) styrene) (PS-b-PMPCS), in p-xylene, a selective solvent at room temperature, was studied. Therod-coil copolymers, which have the same PS length but different PMPCS length, were synthesized by 2,2,6,6-tetramethyl-I-piperidinyloxy (TEMPO) mediated living free radical polymerization. The influence of the rod length on the self-assemblymorphology was studied by transmission electron microscopy (TEM). At a concentration of 2.0 mg/mL, those copolymerswith relatively shorter PMPCS length (copolymers 1 and 2) form individual spherical micelles; those with relatively longerPMPCS length (copolymer 3 and 4) form 'pearl chains' coexisting with individual spherical micelles; the ones with longestPMPCS length form 'pearl chains' coexisting with occasionally formed nanofibers. The diameter of all the morphologieswas controlled by the rod length. This gives us a way to govern the self-assembly morphology by altering the length of oneblock in the block copolymer.
基金financially supported by the National Natural Science Foundation of China(Nos.21174167 and 20974123)the Guangdong Province Higher School Science and Technology Innovation Key Project and the Natural Science Foundation of Guangdong Province(No.S2013030013474)
文摘Herein we demonstrate crystallization-driven self-assembly ofisotactic polystyrene (iPS) with high isotacticity and narrow molecular weight distribution and crystallization-induced switching of the morphology of iPS aggregates in N, N-dimethylformamide (DMF). The formation and morphology switching of the self-assembled aggregates of iPS are investigated by means of dynamic light scattering (DLS), scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and wide angle X-ray diffraction (WXRD). The results reveal that cooling DMF solution of iPS promotes iPS chains to self-assemble into spherical aggregates with a gelled core cross-linked by microcrystals, which is surrounded by solvent-swollen corona. Furthermore, crystallization induces the deformation of iPS aggregates from spherical to plate-like or nest-like.
基金The authors are thankful for financial support from National Science Foundation for Distinguished Young Scholars(51825304)National Natural Science Foundation of China(52122314,51873229 and 51961145103)+3 种基金the project of Bureau of International Cooperation,CAS(121731KYSB20200006)Youth Innovation Promotion Association of CAS(Y2020062)Shanghai Scientific and Technological Innovation Project(19ZR1468400,19590750400,20JC1415400 and 21520780100)Innovation Program of Shanghai Municipal Education Commission(2019-01-07-00-05-E00012).
文摘Fragmentation/disassembly of fiber-like micelles generated by living crystalline-driven self-assembly(CDSA)is usually encountered in aqueous media,which hinders the applications of micelles.Herein,we report the generation of uniform fiber-like micelles consisting of a𝜋Л-conjugated oligo(p-phenylenevinylene)core and a crosslinking silica shell with grafted poly(ethylene glycol)(PEG)chains by the combination of living CDSA,silica chemistry and surface grafting-onto strategy.Owing to the presence of crosslinking silica shell and the outmost PEG chains,the resulting micelles exhibit excellent dispersity and colloidal stability in PBS buffer,BSA aqueous solution and upon heating at 80℃ for 2 h without micellar fragmentation/disassembly.The micelles also show negligible cytotoxicity toward both HeLa cervical cancer and HEK239T human embryonic kidney cell lines.Interestingly,micelles with Ln of 156 nm show the“stealth”property with no significant uptake by HeLa cells,whereas some certain amounts of micelles with Ln of 535 nm can penetrate into HeLa cells,showing length-dependent cellular uptake behaviors.These results provide a route to prepare uniform,colloidally stable fiber-like nanostructures with tunable length and functions derived for biomedical applications.
文摘Supramolecular polymerization properties have been studied for a series of perylene bisimide(PBI)dyes containing identical hydrogen-bonding amide groups in imide positions but variable number or size of alkoxy substituents in bay-positions.
基金supported by the National Natural Science Foundation of China(21905001,21925102,21991132,92056118)the National Key R&D Program of China(2020YFA0908100)+5 种基金Beijing Municipal Natural Science Foundation(L182003)Beijing National Laboratory for Molecular Sciences(BNLMS-CXXM-202006)Guangdong Natural Science Foundation(GDST19EG22)the Science,Technology,and Innovation Commission of Shenzhen Municipality(JCYJ20190813094601656)Clinical Medicine Plus X project of Peking UniversityFundamental Research Funds for the Central Universities。
文摘Information-rich molecules provide opportunities for evolution.Genetically engineered materials are superior in that their properties are coded within genetic sequences and could be fine-tuned.In this review,we elaborate the concept of genetically engineered materials(GEMs)using examples ranging from engineered protein materials to engineered living materials.Proteinbased materials are the materials of choice by nature.Recent progress in protein engineering has led to opportunities to tune their sequences for optimal material performance.Proteins also play a central role in living materials where they act in concert with other biological components as well as nonbiological cofactors,giving rise to living features.While the existing GEMs are often limited to those constructed by building blocks of biological origin,being genetically engineerable does not preclude nonbiologic or synthetic materials,the latter of which have yet to be fully explored.
基金support by the National Natural Science Foundation of China(No.21931003)is gratefully acknowledged.
文摘Block copolymers have aroused much interest,and their application has been rapidly expanded.In recent years,our group has committed to exploring synthesis and self-assembly of block copolymers.We have designed and synthesized several new thermo-responsive polymers and photo-responsive polymers by living/controlled radical polymerization(LCRP)and investigated their stimuli-responsive properties.Aiming at convenient and efficient synthesis of block copolymer nano-assemblies,we have developed several methods based on polymerization-induced self-assembly(PISA).Herein,we give a short summary of our research in these years.The aim of this account is to stimulate innovative synthesis strategies of block copolymer nano-assemblies,and promote more scientific research cooperation to face the exciting opportunities and challenges encountered in block copolymers.