Paige Jacky
@paigejacky.bsky.social
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PhD Candidate in the Fors Group @ Cornell | UNC-Chapel Hill Chemistry '21
reposted by
Paige Jacky
Fors Group
3 months ago
We are so grateful to Synthesis Workshop for hosting Paige Jacky to discuss her stellar work on user-friendly anionic polymerizations! Check it out!
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reposted by
Paige Jacky
Reagan Dreiling
3 months ago
Soooo my best friend is smart *and* internet famous?! Go
@paigejacky.bsky.social
!!!
add a skeleton here at some point
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reposted by
Paige Jacky
Fors Group
3 months ago
💯💯💯 100th paper alert!!! 5th year
@paigejacky.bsky.social
and 3rd year Madison Neukirch have achieved RAFT for anionic polymerization using an aldehyde CTA! What some professors have called "sh*tty aldol chemistry," we call success 😎
doi.org/10.1021/jacs...
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Anionic Reversible Addition–Fragmentation Chain-Transfer Polymerization of Methacrylates
Anionic polymerizations of methacrylates are controlled processes that give well-defined materials; however, these polymerizations require reactive and pyrophoric organolithium reagents for initiation...
https://doi.org/10.1021/jacs.5c10586
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reposted by
Paige Jacky
Fors Group
6 months ago
Maddy, Maeve, and Izzy passed their A exams today and are officially PhD candidates!!
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Truly could not have done it without the support of
@forsgroup.bsky.social
, especially as I learned the hard way that 'bone dry' CO2 is actually not that dry
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7 months ago
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reposted by
Paige Jacky
Fors Group
8 months ago
We come in peace ☮️ 🕊️ Amine you no harm ✋🤚--only selective and controlled polymerization! Using EDA complexes to trigger deamination, 1st author Megan Driscoll initiates photocontrolled polymerization from the α-C of primary amines! (Peptides hate to see Megan coming)
pubs.acs.org/doi/10.1021/...
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Radical Deamination of Primary Amines for Initiation of Controlled Polymerization
Selectively initiating controlled polymerizations using common functional groups is a powerful route to synthesizing advanced polymer architectures. Amines are one of the most common functional groups in small molecules, pharmaceuticals, and biomolecules, and thus are valuable substituents to use for initiating controlled polymerizations. In this study, we present the facile initiation of a controlled radical polymerization from the α-carbon of a primary amine via an electron donor–acceptor (EDA) complex-triggered radical deamination. Through this method, polymers were successfully grafted from a variety of amino acid derivatives. The resulting polymers had good matching between theoretical and experimental molar masses, narrow molar mass distributions (Đ ∼ 1.1–1.2), and exceptional α-chain end fidelities. This method was trialed on a model dipeptide, demonstrating the viability of EDA-RAFT in the synthesis of peptide–polymer conjugates.
https://pubs.acs.org/doi/10.1021/jacs.5c02493
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Un-recyclable thermosets who? Never heard of her. Only recyclable and degradation thermosets here
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11 months ago
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reposted by
Paige Jacky
Reagan Dreiling
11 months ago
As Jon Stewart said, “It is important in these troubled times to continue to dab on the haters” … and the haters would be loathe to see my first independent work on recyclable/degradable thermosets made from 2,3-dihydrofuran! 🌱🥽♻️
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Degradable thermosets via orthogonal polymerizations of a single monomer - Nature
Degradable thermoset multimaterials can be synthesized from a commercially accessible, biosourced monomer using orthogonal polymerizations in a single pot; after selective degredation, the resulting s...
https://www.nature.com/articles/s41586-024-08386-w
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reposted by
Paige Jacky
Fors Group
11 months ago
Oh my 2,3-dihydrofuran, I don’t know know any monomer cooler than Thee. Your cyclic vinyl ether, Makes thermosetting so much easier For me: You ROMP in the dark, Crosslink in the light, Recycle to monomer under vacuum overnight. Degrade in acid or with a lot of O2, Oh DHF this is an ode to you.
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Degradable thermosets via orthogonal polymerizations of a single monomer - Nature
Degradable thermoset multimaterials can be synthesized from a commercially accessible, biosourced monomer using orthogonal polymerizations in a single pot; after selective degredation, the resulting s...
https://www.nature.com/articles/s41586-024-08386-w
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reposted by
Paige Jacky
Fors Group
about 1 year ago
D-d-d-d-drop the Brett 🍾🎈🎉
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reposted by
Paige Jacky
Fors Group
about 1 year ago
What’s up
#chemsky
?! Seems fitting for our first post to be an announcement of the new PhD students in the lab - Lydia Goedert and Nadia Crawford!! Lydia joins us from Stanford U., while Nadia comes from Trinity U. Wish them high yields and low dispersities for their next 5 years! 🥂🎓
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