Robb, Maxwell
- Tseng, Yu-Ling and Zeng, Tian, et el. (2024) Incorporation of a self-immolative spacer enables mechanically triggered dual payload release; Chemical Science; Vol. 15; No. 4; 1472-1479; PMCID PMC10806706; 10.1039/d3sc06359c
- Zeng, Tian and Ordner, Liam A., et el. (2024) Multimechanophore Polymers for Mechanically Triggered Small Molecule Release with Ultrahigh Payload Capacity; Journal of the American Chemical Society; Vol. 146; No. 1; 95-100; 10.1021/jacs.3c11927
- Sun, Yan and McFadden, Molly E., et el. (2023) Anomalous photochromism and mechanochromism of a linear naphthopyran enabled by a polarizing dialkylamine substituent; Chemical Science; Vol. 14; No. 38; 10494-10499; PMCID PMC10548511; 10.1039/d3sc03790h
- McFadden, Molly E. and Barber, Ross W., et el. (2023) Naphthopyran molecular switches and their emergent mechanochemical reactivity; Chemical Science; Vol. 14; No. 37; 10041-10067; PMCID PMC10530568; 10.1039/d3sc03729k
- Yao, Yuxing and McFadden, Molly E., et el. (2023) Remote control of mechanochemical reactions under physiological conditions using biocompatible focused ultrasound; Proceedings of the National Academy of Sciences; Vol. 120; No. 39; e2309822120; PMCID PMC10523651; 10.1073/pnas.2309822120
- Osler, Skylar K. and McFadden, Molly E., et el. (2023) Mechanochemical reactivity of a multimodal 2H-bis-naphthopyran mechanophore; Polymer Chemistry; Vol. 14; No. 22; 2717-2723; 10.1039/D3PY00344B
- McFadden, Molly E. and Overholts, Anna C., et el. (2023) Validation of an Accurate and Expedient Initial Rates Method for Characterizing Mechanophore Reactivity; ACS Macro Letters; Vol. 12; No. 4; 440-445; 10.1021/acsmacrolett.3c00054
- Luo, Stella M. and Barber, Ross W., et el. (2023) Competitive Activation Experiments Reveal Significantly Different Mechanochemical Reactivity of Furan-Maleimide and Anthracene-Maleimide Mechanophores; ACS Polymers Au; Vol. 3; No. 2; 202-208; PMCID PMC10103189; 10.1021/acspolymersau.2c00047
- McFadden, Molly E. and Osler, Skylar K., et el. (2023) Mechanical Force Enables an Anomalous Dual Ring-Opening Re-action of Naphthodipyran; 10.26434/chemrxiv-2022-f8mh3
- Overholts, Anna C. and Granados Razo, Wendy, et el. (2023) Mechanically gated formation of donor–acceptor Stenhouse adducts enabling mechanochemical multicolour soft lithography; Nature Chemistry; Vol. 15; No. 3; 332-338; 10.1038/s41557-022-01126-5
- McFadden, Molly E. and Osler, Skylar K., et el. (2022) Mechanical Force Enables an Anomalous Dual Ring-Opening Reaction of Naphthodipyran; Journal of the American Chemical Society; Vol. 144; No. 49; 22391-22396; 10.1021/jacs.2c08817
- Husic, Corey C. and Hu, Xiaoran, et el. (2022) Incorporation of a Tethered Alcohol Enables Efficient Mechanically Triggered Release in Aprotic Environments; ACS Macro Letters; Vol. 11; No. 8; 948-953; 10.1021/acsmacrolett.2c00344
- Overholts, Anna C. and Robb, Maxwell J. (2022) Examining the Impact of Relative Mechanophore Activity on the Selectivity of Ultrasound-Induced Mechanochemical Chain Scission; ACS Macro Letters; Vol. 11; No. 6; 733-738; 10.1021/acsmacrolett.2c00217
- Overholts, Anna C. and Granados Razo, Wendy, et el. (2022) Mechanically Gated Formation of Donor–Acceptor Stenhouse Adducts Enabling Mechanochemical Multicolor Soft Lithography; 10.26434/chemrxiv-2022-f09r0
- Barber, Ross W. and Robb, Maxwell J. (2022) A 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
- Overholts, Anna C. and McFadden, Molly E., et el. (2022) Quantifying Activation Rates of Scissile Mechanophores and the Influence of Dispersity; Macromolecules; Vol. 55; No. 1; 276-283; 10.1021/acs.macromol.1c02232
- Versaw, Brooke A. and Zeng, Tian, et el. (2021) Harnessing the Power of Force: Development of Mechanophores for Molecular Release; Journal of the American Chemical Society; Vol. 143; No. 51; 21461-21473; 10.1021/jacs.1c11868
- Zeng, Tian and Hu, Xiaoran, et el. (2021) 5-Aryloxy substitution enables efficient mechanically triggered release from a synthetically accessible masked 2-furylcarbinol mechanophore; Chemical Communications; Vol. 57; No. 85; 11173-11176; 10.1039/d1cc04886d
- Osler, Skylar K. and McFadden, Molly E., et el. (2021) Comparison of the reactivity of isomeric 2H- and 3H-naphthopyran mechanophores; Journal of Polymer Science; Vol. 59; No. 21; 2537-2544; 10.1002/pol.20210417
- Barber, Ross W. and Robb, Maxwell J. (2021) A modular approach to mechanically gated photoswitching with color-tunable molecular force probes; Chemical Science; Vol. 12; No. 35; 11703-11709; PMCID PMC8442728; 10.1039/d1sc02890a
- Hu, Xiaoran and Zeng, Tian, et el. (2021) Mechanically Triggered Release of Functionally Diverse Molecular Payloads from Masked 2-Furylcarbinol Derivatives; ACS Central Science; Vol. 7; No. 7; 1216-1224; PMCID PMC8323246; 10.1021/acscentsci.1c00460
- McFadden, Molly E. and Robb, Maxwell J. (2021) Generation 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
- Klein, Isabel M. and Husic, Corey C., et el. (2020) Validation of the CoGEF Method as a Predictive Tool for Polymer Mechanochemistry; Journal of the American Chemical Society; Vol. 142; No. 38; 16364-16381; 10.1021/jacs.0c06868
- Versaw, Brooke A. and McFadden, Molly E., et el. (2020) Designing naphthopyran mechanophores with tunable mechanochromic behavior; Chemical Science; Vol. 11; No. 17; 4525-4530; PMCID PMC8159456; 10.1039/d0sc01359e
- Robb, Maxwell J. (2020) Leveraging polymer mechanics at the molecular scale for chemical reactivity
- Robb, Maxwell J. (2020) Strategic covalent bond transformations using mechanical force
- Hu, Xiaoran and Zeng, Tian, et el. (2019) Mechanically Triggered Small Molecule Release from a Masked Furfuryl Carbonate; Journal of the American Chemical Society; Vol. 141; No. 38; 15018-15023; 10.1021/jacs.9b08663
- Barber, Ross W. and McFadden, Molly E., et el. (2019) Mechanochemically Gated Photoswitching: Expanding the Scope of Polymer Mechanochromism; Synlett; Vol. 30; No. 15; 1725-1732; 10.1055/s-0037-1611858
- Hu, Xiaoran and McFadden, Molly Elizabeth, et el. (2019) Photoswitch generation using mechanical force
- Hu, Xiaoran and Zeng, Tian, et el. (2019) Molecular design strategies for mechanochemically active polymers
- Robb, Maxwell J. (2019) Force-decoupled strategies in mechanochemically active polymers
- McFadden, Molly Elizabeth and Robb, Maxwell J. (2019) Force-dependent color generation using a multifunctional mechanophore
- McFadden, Molly E. and Robb, Maxwell J. (2019) Force-Dependent Multicolor Mechanochromism from a Single Mechanophore; Journal of the American Chemical Society; Vol. 141; No. 29; 11388-11392; 10.1021/jacs.9b05280
- Sulkanen, Audrey R. and Sung, Jaeuk, et el. (2019) Spatially Selective and Density-Controlled Activation of Interfacial Mechanophores; Journal of the American Chemical Society; Vol. 141; No. 9; 4080-4085; 10.1021/jacs.8b10257
- Kim, Tae Ann and Robb, Maxwell J., et el. (2018) Mechanical Reactivity of Two Different Spiropyran Mechanophores in Polydimethylsiloxane; Macromolecules; Vol. 51; No. 22; 9177-9183; 10.1021/acs.macromol.8b01919
- Hu, Xiaoran and McFadden, Molly E., et el. (2018) Mechanochemical Regulation of a Photochemical Reaction; Journal of the American Chemical Society; Vol. 140; No. 43; 14073-14077; 10.1021/jacs.8b09628
- Sung, Jaeuk and Robb, Maxwell J., et el. (2018) Interfacial Mechanophore Activation Using Laser-Induced Stress Waves; Journal of the American Chemical Society; Vol. 140; No. 15; 5000-5003; 10.1021/jacs.8b01427
- Patrick, Jason F. and Robb, Maxwell J., et el. (2016) Polymers with autonomous life-cycle control; Nature; Vol. 540; No. 7633; 363-370; 10.1038/nature21002
- Kortan, Adam M. and Cannizzaro, Randall J., et el. (2016) Poly(ether sulfone)s using a rigid dibenzothiophene dioxide heterocycle; Journal of Polymer Science Part A: Polymer Chemistry; Vol. 54; No. 19; 3127-3131; 10.1002/pola.28197
- Robb, Maxwell J. and Li, Wenle, et el. (2016) A 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
- Robb, Maxwell J. and Kim, Tae Ann, et el. (2016) Regioisomer-Specific Mechanochromism of Naphthopyran in Polymeric Materials; Journal of the American Chemical Society; Vol. 138; No. 38; 12328-12331; 10.1021/jacs.6b07610
- Russ, Boris and Robb, Maxwell J., et el. (2016) Tethered 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
- May, Preston A. and Munaretto, Nicholas F., et el. (2016) Is 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
- Hartmeier, Benjamin F. and Brady, Michael A., et el. (2016) Significance 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
- Handa, Nisha V. and Serrano, Abigail V., et el. (2015) Exploring the synthesis and impact of end‐functional poly(3‐hexylthiophene); Journal of Polymer Science Part A: Polymer Chemistry; Vol. 53; No. 7; 831-841; 10.1002/pola.27522
- Tsurui, Kazuhiko and Murai, Masahito, et el. (2014) Modulating the Properties of Azulene‐Containing Polymers through Controlled Incorporation of Regioisomers; Advanced Functional Materials; Vol. 24; No. 46; 7338-7347; 10.1002/adfm.201402554
- Oh, Seung Soo and Lee, Bongjae F., et el. (2014) Synthetic 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
- Murai, Masuhito and Ku, Sung-Yu, et el. (2014) Modulating structure and properties in organic chromophores: influence of azulene as a building block; Chemical Science; Vol. 5; No. 10; 3753-3760; 10.1039/C4SC01623H
- Robb, Maxwell J. and Newton, Brandon, et el. (2014) One-Step Synthesis of Unsymmetrical N-Alkyl-N′-aryl Perylene Diimides; Journal of Organic Chemistry; Vol. 79; No. 13; 6360-6365; 10.1021/jo500945k
- Russ, Boris and Robb, Maxwell J., et el. (2014) Power Factor Enhancement in Solution‐Processed Organic n‐Type Thermoelectrics Through Molecular Design; Advanced Materials; Vol. 26; No. 21; 3473-3477; 10.1002/adma.201306116
- Robb, Maxwell J. and Ku, Sung-Yu, et el. (2013) 25th Anniversary Article: No Assembly Required: Recent Advances in Fully Conjugated Block Copolymers; Advanced Materials; Vol. 25; No. 40; 5686-5700; 10.1002/adma.201302677
- Klinger, Daniel and Robb, Maxwell J., et el. (2013) Supramolecular 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
- Fors, Brett P. and Poelma, Justin E., et el. (2013) Fabrication 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
- Robb, Maxwell J. and Montarnal, Damien, et el. (2013) A One-Step Strategy for End-Functionalized Donor–Acceptor Conjugated Polymers; Macromolecules; Vol. 46; No. 16; 6431-6438; 10.1021/ma401255d
- MacKenzie, Roderick C. I. and Shuttle, Chris G., et el. (2013) Interpreting 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
- Robb, Maxwell J. and Ku, Sung-Yu, et el. (2013) A 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
- Connal, Luke A. and Lynd, Nathaniel A., et el. (2012) Mesostructured Block Copolymer Nanoparticles: Versatile Templates for Hybrid Inorganic/Organic Nanostructures; Chemistry of Materials; Vol. 24; No. 21; 4036-4042; PMCID PMC3546830; 10.1021/cm3011524
- Ku, Sung-Yu and Brady, Michael A., et el. (2012) A Modular Strategy for Fully Conjugated Donor–Acceptor Block Copolymers; Journal of the American Chemical Society; Vol. 134; No. 38; 16040-16046; 10.1021/ja307431k
- Robb, Maxwell J. and Connal, Luke A., et el. (2012) Functional block copolymer nanoparticles: toward the next generation of delivery vehicles; Polymer Chemistry; Vol. 3; No. 6; 1616-1628; PMCID PMC4257844; 10.1039/C2PY20131C
- Lo Conte, Mauro and Robb, Maxwell J., et el. (2011) Exhaustive 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
- Lin, Brian F. and Marullo, Rachel S., et el. (2011) De Novo Design of Bioactive Protein-Resembling Nanospheres via Dendrimer-Templated Peptide Amphiphile Assembly; Nano Letters; Vol. 11; No. 9; 3946-3950; PMCID PMC3223106; 10.1021/nl202220q
- Antoni, Per and Robb, Maxwell J., et el. (2010) Pushing 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
- Robb, Maxwell J. and Hawker, Craig J. (2006) "Click" Chemistry in Polymer Science: CuAAC and Thiol–Ene Coupling for the Synthesis and Functionalization of Macromolecules; ISBN 9783527313952; Materials Science and Technology: a Comprehensive Treatment; 10.1002/9783527603978.mst0440