2019
DOI: 10.1039/c9sc03756j
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Orthogonal functionalization of alternating polyesters: selective patterning of (AB)n sequences

Abstract: A series of AB alternating polyesters are orthogonally patterned to install two different functionalities at regular intervals along the backbone and with high precision.

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Cited by 46 publications
(63 citation statements)
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References 72 publications
(87 reference statements)
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“…Then the internal alkenes were quantitatively converted into carboxylic acids, amines, alkyl, and oligo-groups groups by thiol-ene reactions. These copolymers with both hydrophobic and hydrophilic blocks can be self-assembled into nanostructures in aqueous solution, which is expected to be used as antimicrobial agents and biodegradable drug delivery vehicles (Yi et al, 2019). Sanford et al used vanillin glycidyl ether (VGE) to directly introduce aldehyde functional group into the polymer chain by copolymerizing with PO and carbic anhydride (CPMA), using the [( F salph)Al(THF)][OTf]/[PPN] 2 [ADC] as a bifunctional catalytic system.…”
Section: Post-polymerization Modification Of Polymers Obtained By Ring-opening Copolymerizationmentioning
confidence: 99%
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“…Then the internal alkenes were quantitatively converted into carboxylic acids, amines, alkyl, and oligo-groups groups by thiol-ene reactions. These copolymers with both hydrophobic and hydrophilic blocks can be self-assembled into nanostructures in aqueous solution, which is expected to be used as antimicrobial agents and biodegradable drug delivery vehicles (Yi et al, 2019). Sanford et al used vanillin glycidyl ether (VGE) to directly introduce aldehyde functional group into the polymer chain by copolymerizing with PO and carbic anhydride (CPMA), using the [( F salph)Al(THF)][OTf]/[PPN] 2 [ADC] as a bifunctional catalytic system.…”
Section: Post-polymerization Modification Of Polymers Obtained By Ring-opening Copolymerizationmentioning
confidence: 99%
“…Besides, the coexistence of species with different degrees of functionality usually leads to broad or even multimodal molecular weight distributions, which also jeopardizes the chain-end fidelity. Moreover, excessive protonic functional groups may cause catalyst deactivation (Yi et al, 2019). Therefore, post-polymerization modification is an important means to realize multi-functionalities on ROCOP polymers, and the desired functional groups can be accurately connected to the polymer chain by different modification methods (Ntoukam et al, 2020).…”
Section: Introductionmentioning
confidence: 99%
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“…[18][19][20][21] Due to their attractive phase separation behaviors, which promise a wide scope of applications, block copolymers incorporated with mechanistically incompatible monomers are of special research interest. [22][23][24][25][26][27] It can be envisioned that tandem catalysis permits exceptional efficiency in the synthesis of block copolymers from monomer mixtures by integrating different polymerization cycles in a one-pot process. However, most of the research efforts in such attempts are dependent on orthogonal tandem catalysis.…”
Section: Introductionmentioning
confidence: 99%
“…[16][17][18] The groups of Yang [19] and Maser [20] also confirmed the crosslinkinge nhanced emission (CEE) effect that the hydrogen-bond-mediated supramolecular interactions from the FSGs controla nd facilitate the photoluminescence of PDs. Different types or degrees of carbonizedc ore and distinct interactions of FSG could induce unprecedented spatial organization, folding, and self-assembly, [21] changing the surfaces tate, core, and size of PDs, whicha re suspected of contributing to the photoluminescent tunability [22,23] including improvement in QY and shift in emission wavelength. [24,25] Moreover,t here are also reports [22,26] of regulating the emission wavelength by controlling the particle size [5,27] of PDs.…”
Section: Introductionmentioning
confidence: 99%