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Chemical Structure| 2069-41-2 Chemical Structure| 2069-41-2

Structure of 2069-41-2

Chemical Structure| 2069-41-2

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Product Citations

Product Citations

Wu, Yukun ;

Abstract: The growing environmental impact of plastic pollution has intensified the demand for sustainable polymer systems that combine high performance, processability, and environmental responsibility. This thesis presents innovative molecular design strategies for creating functional and recyclable polymers by integrating synthetic chemistry with emerging tools in artificial intelligence (AI). First, a series of luminescent polymers based on the thermally activated delayed fluorescence (TADF) mechanism were synthesized by incorporating cleavable tert-butyl ester groups into the polymer backbones, enabling controlled depolymerization and refunctionalization without compromising light-emitting efficiency. Beyond electroactive materials, the second part addresses the recycling challenges of traditional plastics, particularly the poor compatibility of mixed polymer waste. To overcome this, universal linkers containing reversible dynamic bonds and azide end groups were developed to chemically bond with inert polymers, forming compatible phases within immiscible polymer blends. These linkers significantly improved mechanical properties and enabled multiple cycles of mechanical recycling with minimal performance loss. In the final section, AI and automation were applied to accelerate the discovery of electrochromic polymers (ECPs) through a closed-loop platform that integrates machine learning (ML), predictive modeling, and robotic synthesis, enabling efficient inverse design and rapid material development. Collectively, this work demonstrates how smart molecular design, dynamic bonding strategies, and AI-driven discovery can be combined to advance sustainable materials, supporting the vision of a circular polymer economy.

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Product Details of [ 2069-41-2 ]

CAS No. :2069-41-2
Formula : C13H8BrFO
M.W : 279.10
SMILES Code : O=C(C1=CC=C(Br)C=C1)C2=CC=C(F)C=C2
MDL No. :MFCD00672035
InChI Key :SSXSFTBOKUQUAX-UHFFFAOYSA-N
Pubchem ID :74951

Safety of [ 2069-41-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 2069-41-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 2069-41-2 ]
 

Historical Records

Technical Information

• Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Benzylic Oxidation • Birch Reduction • Blanc Chloromethylation • Bucherer-Bergs Reaction • Clemmensen Reduction • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Fischer Indole Synthesis • Friedel-Crafts Reaction • General Reactivity • Grignard Reaction • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Hydrogenolysis of Benzyl Ether • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Lawesson's Reagent • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Alkylbenzene • Preparation of Amines • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Dihalides • Reformatsky Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Vilsmeier-Haack Reaction • Wittig Reaction • Wolff-Kishner Reduction

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