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photochromism and mechanochromism of a linear naphthopyran enabled by a
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control of mechanochemical reactions under physiological conditions
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of an Accurate and Expedient Initial Rates Method for Characterizing
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Activation Experiments Reveal Significantly Different Mechanochemical
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Force Enables an Anomalous Dual Ring-Opening Re-action of
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Force Enables an Anomalous Dual Ring-Opening Reaction of
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of a Tethered Alcohol Enables Efficient Mechanically Triggered Release
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the Impact of Relative Mechanophore Activity on the Selectivity of
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mechanochemical two for one: Mechanical activation of norborn‐2‐en‐7‐one
releases carbon monoxide and switches on aggregation‐induced
emission; Aggregate; Vol. 3; No. 2; Art. No. e196; 10.1002/agt2.196
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substitution enables efficient mechanically triggered release from a
synthetically accessible masked 2-furylcarbinol mechanophore;
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of the reactivity of isomeric 2H- and 3H-naphthopyran mechanophores;
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modular approach to mechanically gated photoswitching with color-tunable
molecular force probes; Chemical Science; Vol. 12; No. 35;
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of an Elusive Permanent Merocyanine via a Unique Mechanochemical
Reaction Pathway; Journal of the American Chemical Society; Vol.
143; No. 21; 7925-7929; 10.1021/jacs.1c03865
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polymer mechanics at the molecular scale for chemical
reactivity
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covalent bond transformations using mechanical force
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Triggered Small Molecule Release from a Masked Furfuryl Carbonate;
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strategies in mechanochemically active polymers
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color generation using a multifunctional mechanophore
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design strategies for mechanochemically active polymers
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generation using mechanical force
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Multicolor Mechanochromism from a Single Mechanophore; Journal of
the American Chemical Society; Vol. 141; No. 29; 11388-11392; 10.1021/jacs.9b05280
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Selective and Density-Controlled Activation of Interfacial
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Reactivity of Two Different Spiropyran Mechanophores in
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Regulation of a Photochemical Reaction; Journal of the American
Chemical Society; Vol. 140; No. 43; 14073-14077; 10.1021/jacs.8b09628
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Mechanophore Activation Using Laser-Induced Stress Waves; Journal of
the American Chemical Society; Vol. 140; No. 15; 5000-5003; 10.1021/jacs.8b01427
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with autonomous life-cycle control; Nature; Vol. 540; No. 7633;
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sulfone)s using a rigid dibenzothiophene dioxide heterocycle;
Journal of Polymer Science Part A: Polymer Chemistry; Vol. 54; No. 19;
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Robust Damage-Reporting Strategy for Polymeric Materials Enabled by
Aggregation-Induced Emission; ACS Central Science; Vol. 2; No. 9;
598-603; PMCID PMC5043436; 10.1021/acscentsci.6b00198
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Mechanochromism of Naphthopyran in Polymeric Materials; Journal of
the American Chemical Society; Vol. 138; No. 38; 12328-12331; 10.1021/jacs.6b07610
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tertiary amines as solid-state n-type dopants for solution-processable
organic semiconductors; Chemical Science; Vol. 7; No. 3; 1914-1919;
PMCID PMC5966797; 10.1039/c5sc04217h
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Molecular Weight or Degree of Polymerization a Better Descriptor of
Ultrasound-Induced Mechanochemical Transduction?; ACS Macro Letters;
Vol. 5; No. 2; 177-180; 10.1021/acsmacrolett.5b00855
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of miscibility in multidonor bulk heterojunction solar cells;
Journal of Polymer Science, Part B: Polymer Physics; Vol. 54; No. 2;
237-246; 10.1002/polb.23907
- Robb, Maxwell J. and Moore, Jeffrey S. (2015) A
Retro-Staudinger Cycloaddition: Mechanochemical Cycloelimination of a
β-Lactam Mechanophore; Journal of the American Chemical Society;
Vol. 137; No. 34; 10946-10949; 10.1021/jacs.5b07345
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the synthesis and impact of end‐functional poly(3‐hexylthiophene);
Journal of Polymer Science Part A: Polymer Chemistry; Vol. 53; No. 7;
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the Properties of Azulene‐Containing Polymers through Controlled
Incorporation of Regioisomers; Advanced Functional Materials; Vol.
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Aptamer-Polymer Hybrid Constructs for Programmed Drug Delivery into
Specific Target Cells; Journal of the American Chemical Society;
Vol. 136; No. 42; 15010-15015; PMCID PMC4210129; 10.1021/ja5079464
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structure and properties in organic chromophores: influence of azulene
as a building block; Chemical Science; Vol. 5; No. 10; 3753-3760; 10.1039/C4SC01623H
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Synthesis of Unsymmetrical N-Alkyl-N′-aryl Perylene Diimides;
Journal of Organic Chemistry; Vol. 79; No. 13; 6360-6365; 10.1021/jo500945k
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Factor Enhancement in Solution‐Processed Organic n‐Type Thermoelectrics
Through Molecular Design; Advanced Materials; Vol. 26; No. 21;
3473-3477; 10.1002/adma.201306116
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Anniversary Article: No Assembly Required: Recent Advances in Fully
Conjugated Block Copolymers; Advanced Materials; Vol. 25; No. 40;
5686-5700; 10.1002/adma.201302677
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guests in solvent driven block copolymer assembly: from internally
structured nanoparticles to micelles; Polymer Chemistry; Vol. 4;
No. 19; 5038-5042; PMCID PMC4267284; 10.1039/C3PY00750B
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of Unique Chemical Patterns and Concentration Gradients with Visible
Light; Journal of the American Chemical Society; Vol. 135; No. 38;
14106-14109; 10.1021/ja408467b
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One-Step Strategy for End-Functionalized Donor–Acceptor Conjugated
Polymers; Macromolecules; Vol. 46; No. 16; 6431-6438; 10.1021/ma401255d
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the Density of States Extracted from Organic Solar Cells Using Transient
Photocurrent Measurements; Journal of Physical Chemistry C; Vol.
117; No. 24; 12407-12414; 10.1021/jp4010828
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renaissance of color: New structures and building blocks for organic
electronics; Journal of Polymer Science Part A: Polymer Chemistry;
Vol. 51; No. 6; 1263-1271; 10.1002/pola.26531
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Block Copolymer Nanoparticles: Versatile Templates for Hybrid
Inorganic/Organic Nanostructures; Chemistry of Materials; Vol. 24;
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Modular Strategy for Fully Conjugated Donor–Acceptor Block
Copolymers; Journal of the American Chemical Society; Vol. 134;
No. 38; 16040-16046; 10.1021/ja307431k
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block copolymer nanoparticles: toward the next generation of delivery
vehicles; Polymer Chemistry; Vol. 3; No. 6; 1616-1628; PMCID
PMC4257844; 10.1039/C2PY20131C
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glycosylation, pegylation, and glutathionylation of a [G4]‐ene_(48)
dendrimer via photoinduced thiol‐ene coupling; Journal of Polymer
Science Part A: Polymer Chemistry; Vol. 49; No. 20; 4468-4475; PMCID
PMC3181107; 10.1002/pola.24888
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Novo Design of Bioactive Protein-Resembling Nanospheres via
Dendrimer-Templated Peptide Amphiphile Assembly; Nano Letters; Vol.
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the Limits for Thiol−Ene and CuAAC Reactions: Synthesis of a 6th
Generation Dendrimer in a Single Day; Macromolecules; Vol. 43;
No. 16; 6625-6631; 10.1021/ma101242u
- Robb, Maxwell J. and Knauss, Daniel M. (2009) Poly(arylene
sulfide)s by nucleophilic aromatic substitution polymerization of
2,7‐difluorothianthrene; Journal of Polymer Science Part A: Polymer
Chemistry; Vol. 47; No. 9; 2453-2461; 10.1002/pola.23341
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Chemistry in Polymer Science: CuAAC and Thiol–Ene Coupling for the
Synthesis and Functionalization of Macromolecules; ISBN
9783527313952; 10.1002/9783527603978.mst0440