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‡(169) Precision Epitaxy for Aqueous 1D and 2D Poly(-caprolactone) Assemblies, M. C. Arno, M. Inam, Z. Coe, G. Cambridge, L. J. Macdougall, R. Keogh, A. P. Dove and R. K. O’Reilly and Rachel K. O’Reilly, J. Am. Chem. Soc, 2017, accepted, DOI: 10.1021/jacs.7b10199

‡(168) The Application of Blocked Isocyanate Chemistry in the Development of Tunable Thermoresponsive Crosslinkers, M. S. Rolph, M. Inam and R. K. O’Reilly, Polym Chem, 2017, accepted, DOI:10.1039/C7PY01706E

‡(167) Permeable Protein-Loaded Polymersome Cascade Nanoreactors by Polymerization-Induced Self-Assembly, L. D. Blackman, S. Varlas, M. C. Arno, A. Fayter, M. I. Gibson , and R. K. O’Reilly, ACS Macro Lett., 2017, 6, 1263–1267, DOI: 10.1021/acsmacrolett.7b00725

‡(166) Evolution of DNA Templated Synthesis as a Tool for Materials Discovery, R. K. O’Reilly, A.J. Turberfield and T.R. Wilks, Acc. Chem. Res., 2017, accepted, DOI: 10.1021/acs.accounts.7b00280.

‡(165) A First Step Towards a Universal Fluorescent Probe: Unravelling the Photodynamics of an Amino-Maleimide Fluorophore, M. Staniforth, W.-D. Quan, T. Karsili, L. Baker, R. K. O’Reilly and V. Stavros, J. Phys. Chem. Part A, 2017, 121, 6357-6365, DOI: 10.1021/acs.jpca.7b04702

‡(164) Understanding the CDSA of poly(lactide) containing triblock copolymers, W. Yu, M. Inam, J.R. Jones, A.P. Dove and R. K. O’Reilly, Polym. Chem, 2017, 8, 5504-5512, DOI: 10.1039/C7PY01056G

‡(163) Thermally Switching On/Off the Hardening of Soaked Nanocomposite Materials, M. M. Pérez-Madrigal, R. K. O’Reilly, ACS Central Science, 2017, 3, 817-819, DOI:10.1021/acscentsci.7b0030

‡(162) Poly(oligo (ethylene glycol) vinyl acetate)s: A versatile new class of thermoresponsive and biocompatible polymers, G. G. Hedir, M. C. Arno, M. Langlais, J. T. Husband, R. K. O’Reilly and A. P. Dove, Angew. Chem. Int. Ed. 2017, 56, 9178-9182, DOI:10.1002/anie.201703763

‡(161) Dispersity Effects in Polymer Self-Assemblies: A Matter of Hierarchical Control, K. E. B. Doncom, L. D. Blackman, D. B. Wright, M. I. Gibson, and R. K. O’Reilly, Chem. Soc. Rev. 2017, 46, 4119-4134, DOI:10.1039/C6CS00818F.

‡(160) One-pot synthesis of micron-sized polybetaine particles; innovative use of supercritical carbon dioxide, H. Willcock, S. P. Bassett, N. A. Birkin, J. Jennings, E. Chapman, R. K. O’Reilly, S. M. Howdle, Polym. Chem., 2017, 8, 4557-4564, DOI: 10.1039/C7PY00455A.

‡(159) Dispersion of Single-Walled Carbon Nanotubes Using Nucleobase-Containing Poly(acrylamide) Polymers, D. Fong, Z. Hua, T. R. Wilks, R. K. O’Reilly and A. Adronov, J. Polym. Sci. Part A: Polym Chem, 2017, 55, 2611-2617, DOI: 10.1002/pola.28652.

‡(158) Comparison of photo- and thermally initiated polymerization-induced self-assembly; lack of end group fidelity drives the formation of higher order morphologies, L. Blackman, K.E.B. Doncom, M.I. Gibson and R.K. O'Reilly, Polym. Chem., 2017, 8, 2860 - 2871, DOI: 10.1039/C7PY00407A

‡(157) Reversibly Manipulating the Surface Chemistry of Polymeric Nanostructures via a “Grafting To” Approach Mediated by Nucleobase Interactions, Z. Hua, R. Keogh, Z. Li, T. R. Wilks, G. Chen , and R. K. O’Reilly, Macromolecules, 2017, 50, 3662–3670, DOI: 10.1021/acs.macromol.7b00286

‡(156) Polyelectrolyte pKa from experiment and molecular dynamics simulation, M.S. Bodnarchuk, K.E.B. Doncom, D.B. Wright, D.M. Heyes, D. Dini and R.K. O'Reilly, RSC Adv., 2017, 7, 20007-20014, DOI: 10.1039/C6RA27785C

‡(155) 1D vs. 2D shape selectivity in the crystallization-driven self-assembly of polylactide block copolymers, M. Inam, G.Cambridge, A.Pitto-Barry, Z.P. L. Laker, N.R. Wilson, R.T. Mathers, A.P. Dove and R.K. O'Reilly, Chem Sci, 2017, 8, 4223-4230, DOI: 10.1039/C7SC00641A

‡(154) The hydrolytic behavior of N,N'-(dimethylamino) ethyl acrylate-functionalized polymeric stars, M. S. Rolph, A. Pitto-Barry and R. K. O'Reilly, Polym. Chem., 2017, 8, 5060-5070, DOI: 10.1039/C7PY00219J

‡(153) Probing the Causes of Thermal Hysteresis Using Tunable Nagg Micelles with Linear and Brush-Like Thermoresponsive Coronas, L. D. Blackman, M. I. Gibson and R. K. O’Reilly, Polym. Chem, 2017, 8, 233-244, DOI:

‡(150) The direct synthesis of sulfobetaine-containing amphiphilic block copolymers and their self-assembly behavior, K. E. B. Doncom, H. Willcock, R. K. O’Reilly, Eur. Polym. J., 2017, 87, 497-507, DOI: 10.1016/j.eurpolymj.2016.09.002


‡(151) Efficient DNA-Polymer coupling in organic solvents: a survey of amide coupling, thiol-ene and tetrazine-norbornene chemistries applied to conjugation of poly(n-isopropylacrylamide), T. R. Wilks and R. K. O’Reilly, Sci. Rep., 2016, 6, 39192; DOI: 10.1038/srep39192

‡(150) Blocked isocyanates: from analytical and experimental considerations to non-polyurethane applications, M. S. Rolph, A. L. J. Markowska, C. N. Warriner and R. K. O'Reilly, Polym. Chem., 2016, 7, 7351-7364, DOI:10.1039/c6py01776B

(149) Fluorescent Polymeric Nanovehicles for Neural Stem Cell Modulation, S. A. Papadimitriou, M. P. Robin, D. Ceric, R. K. O'Reilly, S. Marinoc and M. Resmini, Nanoscale, 2016, 8, 1740 - 17349, DOI: 10.1039/C6NR06440J

(148) Scalable synthesis of multicolour conjugated polymer nanoparticles via Suzuki-Miyaura polymerisation in a miniemulsion and application in bioimaging, J. M. Behrendt, J. A. Esquivel Guzman, L. Purdie, H. Willcock, J. J. Morrison, A. B. Foster, R. K. O'Reilly, M. C. McCairn, M. L. Turner, Reactive and Functional Polymers, 2016, 107, 69-77, DOI: 10.1016/j.reactfunctpolym.2016.08.006

‡(147) CO2/pH-responsive particles with built-in fluorescence read-out, A. B. Mabire, Q. Brouard, A. Pitto-Barry, R. J. Williams, H. Willcock, N. Kirby, E. Chapman, R. K. O'Reilly, Polym. Chem., 2016, 7, 5943, DOI: 10.1039/C6PY01254J

‡(146) Shape effect of glyco-nanoparticles on macrophage cellular uptake and immune response, Z. Li, L. Sun, Y. Zhang, A. P. Dove, R. K. O'Reilly, G. Chen, ACS Macro Lett., 2016, 5, 1059-1064, DOI: 10.1021/acsmacrolett.6b00419

‡(145) Micellar nanoparticles with tuneable morphologies through interactions between nucleobase-containing synthetic polymers in aqueous solution, Z. Hua, A. Pitto-Barry, Y. Kang, N. Kirby, T. R. Wilks, R. K. O'Reilly, Polym. Chem.,2016, 7, 4254-4262, DOI: 10.1039/C6PY00716C

(144) Robust bifunctional buckypapers from carbon nanotubes and polynorbornene copolymers for flexible engineering of enzymatic bioelectrodes, A. J. Gross, M. P. Robin, Y. Nedellec, R. K. O'Reilly, D. Shan, S. Cosnier, Carbon, 2016, 107, 542-547, DOI: 10.1016/j.carbon.2016.06.027

‡(143) Use of complementary nucleobase-containing synthetic polymers to prepare complex self-assembled morphologies in water, Y. Kang, A. Pitto-Barry, M. Rolph, Z.Hua, I. Hands-Portman, N.Kirby and R.K.O'Reilly, Polym. Chem. 2016, 7, 2836-2846, DOI: 10.1039/c6py00263c

(142) An autonomous molecular assembler for programmable chemical synthesis, Wenjing Meng, R. A. Muscat, M. L. McKee, P. J. Milnes, A. H. El-Sagheer, J. Bath, B. G. Davis, T. Brown, R. K. O'Reilly and A. J. Turberfield, Nature Chemistry, 2016, 8, 542–548, DOI: 10.1038/NChem.2495

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‡(141) Cyclic Graft Copolymer Unimolecular Micelles: Effects of Cyclization on Particle Morphology and Thermoresponsive Behavior, R. J. Williams, A. Pitto-Barry, N. Kirby, A. P. Dove, and R. K. O’Reilly, Macromolecules, 2016, 49, 2802–2813, DOI: 10.1021/acs.macromol.5b02710

‡(140) Core Functionalization of Semi-Crystalline Polymeric Cylindrical Nanoparticles Using Photo-initiated Thiol-ene Radical Reactions, L. Sun, A. Pitto Barry, A. W. Thomas, M. Inam, K. Doncom, A.P. Dove, R.K. O'Reilly, Polym. Chem., 2016, 7, 2337 - 2341, DOI: 10.1039/C5PY01970B

‡(139) Blending block copolymer micelles in solution; obstacles of blending,
D. B. Wright, J. P. Patterson, N. C. Gianneschi, C. Chassenieux, O. Colombani and R.l K. O'Reilly, Polym. Chem., 2016, 7, 1577-1583, DOI: 10.1039/C5PY02006A

‡(138) Discussion on “Aperiodic Copolymers”, S. J. Rowan, C. Barner-Kowollik, B. Klumperman, P. Gaspard, R. B. Grubbs, M. A. Hillmyer, L. R. Hutchings, M. K. Mahanthappa, D. Moatsou, R. K. O’Reilly, M. Ouchi, M. Sawamoto, and T. P. Lodge, ACS Macro Lett., 2016, 5 (1), 1–3. DOI: 10.1021/acsmacrolett.5b00758

‡(137) Fluorescent Block Copolymer Micelles That Can Self-Report on Their Assembly and Small Molecule Encapsulation, M.P. Robin, S. Osborne, Z. Pikramenou, J. E. Raymond, R. K. O'Reilly, Macromolecules 2016, 49, 653–662, DOI: 10.1021/acs.macromol.5b02152

‡(136) Block Copolymers: Controlling Nanostructure to Generate Functional Materials – Synthesis, Characterization, and Engineering, T.H. Epps III, R. K. O'Reilly, Chem. Sci. 2016, 7, 1674-1689 DOI: 10.1039/C5SC03505H

‡(135) Retaining Individualities: the Photodynamics of Self-Ordering Porphyrin Assemblies, W.D. Quan, A. Pitto-Barry, L.A. Baker, E. Stulz, R. Napier, R.K. O'Reilly, V.G. Stavros, Chem. Commun., 2016, 52, 1938-1941 DOI: 10.1039/C5CC09095D

‡(134) Degradable Precision Polynorbornenes via Ring-Opening Metathesis Polymerization, D. Moatsou, A. Nagarkar, A. F. M. Kilbinger, R. K. O’Reilly, J. Polym. Sci. Part A: Polym. Chem, 2016, DOI: 10.1002/pola.27964.


‡(133) The Copolymer Blending Method: A New Approach for Targeted Assembly of Micellar Nanoparticles, D. B. Wright, J. P. Patterson, A. Pitto-Barry, A. Lu, N. Kirby, N. C. Gianneschi, C. Chassenieux, O. Colombani, and R. K. O’Reilly, Macromolecules, 2015, 48, 6516–6522. DOI: 10.1021/acs.macromol.5b01426

‡(132) The Effect of Micellization on the Thermoresponsive Behavior of Polymeric Assemblies, L.D. Blackman, D. B. Wright, M. P. Robin, M. I. Gibson, R.K.O'Reilly, ACS Macro Letters, 2015, 4, 1210-1214. DOI: 10.1021/acsmacrolett.5b00551

‡(131) Amphiphilic Block Copolymer Self-Assemblies of Poly(NVP)-b-poly(MDO-co-vinyl esters): Tunable Dimensions and Functionalities, G. G. Hedir, A. Pitto-Barry, A. P. Dove, R.K.O'Reilly, J. Polym. Sci. Part A: Polym. Chem, 2015, 53, 2699-2710, DOI: 10.1002/pola.27915

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‡(130) Controlling the synthesis of degradable vinyl polymers by xanthate-mediated polymerization, C. A. Bell, G. G. Hedir, R. K. O'Reilly and A. P. Dove, Polymer Chemistry, 2015, 6, 7447-7454. DOI: 10.1039/c5py01156f 

‡(129) Self-assembly of temperature-responsive protein-polymer bioconjugates, D. Moatsou, J. Li, A. Ranji, A. Pitto-Barry, I. Ntai, M.C. Jewett, R.K. O'Reilly, Bioconjugate Chem, 2015, 26, 1890-1899. DOI: 10.1021/acs.bioconjchem.5b00264

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(128) Osmium Atoms and Os2 Molecules Move Faster on Selenium-doped Compared to Sulfur-doped Boronic Graphenic Surfaces, N. Barry, A. Pitto-Barry, J. Tran, S. Spencer, A. Johansen, A.M. Sanchez, A.P. Dove, R.K. O’Reilly, R. Deeth, R. Beanland, P. Sadler, Chem Mater, 2015, 27, 5100-5105, DOI: 10.1021/acs.chemmater.5b01853

‡(127) RAFT dispersion polymerization: A method to tune the morphology of thymine-containing self-assemblies, Y. Kang, A. Pitto-Barry, A. Maitland, and R. K. O’Reilly, Polymer Chemistry, 2015, 4984 - 4992, DOI: 10.1039/C5PY00617A

‡(126) Functional Degradable Polymers by Radical Ring-Opening Copolymerization of MDO and Vinyl Bromobutanoate: Synthesis, Degradability and Post-Polymerization Modification, G. G. Hedir, C. A. Bell, R. K. O’Reilly, A. P. Dove, Biomacromolecules, 2015, 7, 2049–2058, DOI: 10.1021/acs.biomac.5b00476

(125) Biofunctionalizable flexible bucky paper by combination of multi-walled carbon nanotubes and polynorbornene-pyrene - Application to the bioelectrocatalytic reduction of oxygen, S. Cosnier, R. Haddada, D. Moatsou, R. K. O’Reilly, Carbon, 2015, 93, 713-718. DOI: 10.1016/j.carbon.2015.05.099

‡(124) Aminomaleimide fluorophores: A simple functional group with bright, solvent dependent emission, A. B. Mabire, M. P. Robin, W.-D. Quan, H. Willcock, V. G. Stavros, R. K. O’Reilly, Chem. Commun, 2015, 51, 9733-9736, DOI: 10.1039/C5CC02908B

‡(123) Complementary light scattering and synchrotron small angle X-ray scattering studies of the micelle-to-unimer transition of polysulfobetaines, K.E.B. Doncom, A. Pitto-Barry, H. Willcock, A. Lu, B.E. McKenzie, N. Kirby, R.K. O'Reilly, Soft Matter, 2015, 11, 3666-3676 DOI: 10.1039/C5SM00602C

‡(122) Self-assembly of cyclic polymers, R.J. Williams, A.P. Dove, R.K. O'Reilly, Polymer Chemistry, 2015, 6, 2998-3008 DOI: 10.1039/C5PY00081E

(121) Controlled assembly of artificial protein-protein complexes via DNA duplex formation, E. Ploskon, S. Wagner, A. Ellington, M. Jewett, R. O’Reilly, P. Booth, Bioconjugate Chem. 2015, 26, 427–434 DOI: 10.1021/bc500473s

‡(120) Tuning the aggregation behaviour of pH responsive micelles by copolymerization, D. B. Wright, J. P. Patterson, A. Pitto-Barry, P. Cotanda, C. Chassenieux, O. Colombani, and R. K. O’Reilly, Polymer Chemistry, 2015, 6, 2761-2768 DOI: 10.1039/C4PY01782J

‡(119) Graphene Oxide Single Sheets as Substrate for High Resolution cryoTEM, M.W.P. van de Put, J.P. Patterson, P.H.H. Bomans, H. Friedrich, R.A.T.M. van Benthem, G. de With, R.K. O’Reilly, N.A.J.M. Sommerdijk, Soft Matter, 2015, 11, 1265-1270, DOI: 10.1039/C4SM02587C

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‡(118) Strategies for preparing fluorescently-labelled polymer nanoparticles, M. P. Robin, R.K. O'Reilly, Polym. Inter., 2015, 64, 172-184, DOI: 10.1002/pi.4842.

‡(117) One-pot synthesis of super-bright fluorescent nanogel contrast agents containing a dithiomaleimide fluorophore, M.P. Robin, J.E. Raymond and R.K. O'Reilly, Materials Horizons, 2015, 2, 54-59, DOI: 10.1039/C4MH00167B

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‡(116) Exploiting nucleobase-containing materials – from monomers to complex morphologies using RAFT dispersion polymerization, Y. Kang, A. Pitto-Barry, H. Willcock, W-D Quan, N. Kirby, A. M. Sanchez and R. K. O’Reilly, Polym. Chem., 2015, 6, 106-117
DOI: 10.1039/C4PY01074D

‡(115) The effect of polymer nanostructure on diffusion of small molecules using tryptophan as a FRET probe, B. L. Moore, A. Lu, D. Moatsou, R. K. O’Reilly, Eur. Polym. J., 2015, 62, 380-385, DOI: 10.1016/j.eurpolymj.2014.06.003


‡(114) Recyclable l-Proline Functional Nanoreactors with Temperature-Tuned Activity Based on CoreShell Nanogels, A. Lu, D. Moatsou, I. Hands-Portman, D.A. Longbottom, R.K. O'Reilly, ACS Macro Letters, 2014, 3, 1235-1239, DOI: 10.1021/mz500704y.

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‡(113) Structural Reorganization of Cylindrical Nanoparticles Triggered by Polylactide Stereocomplexation, L. Sun, A. Pitto-Barry, N. Kirby, T. Schiller, A. Sanchez, M. Dyson, J. Sloan, N. Wilson, R.K. O'Reilly, and A.P. Dove, Nature Commun, 2014, 5, 5746. DOI: 10.1038/ncomms6746

‡(112) Dual effect of thiol addition on fluorescent polymeric micelles: ON-to-OFF emissive switch and morphology transition, A. B. Mabire, M.P. Robin, H. Willcock, A. Pitto-Barry, N Kirby and R.K. O'Reilly, Chem. Commun. 2014, 50, 11492-11495, DOI: 10.1039/c4cc04713c.

(111) Precious metal carborane polymer nanoparticles: characterisation of micellar formulations and anticancer activity, N. P. E. Barry, A. Pitto-Barry, I. Romero-Canelón, J. Tran, J. J. Soldevila-Barreda, I. Hands-Portman, C. J. Smith, N. Kirby, A. P. Dove, R. K. O'Reilly and P.J. Sadler, Faraday Discussions. 2014, DOI: 10.1039/c4fd00098f.

‡(110) The pH induced vesicle to micelle morphology transition of a THP-protected polymer , K. E. B. Doncom, H. Willcock and R.K. O'Reilly, J. Polym. Sci. Part A: Polym. Chem, 2014, 52, 3026–3031, DOI: 10.1002/pola.27348.

‡(109) Fluorescent and chemico-fluorescent responsive polymers from dithiomaleimide and dibromomaleimide functional monomers, M.P. Robin and R.K. O'Reilly, Chem. Sci. 2014, 5, 2717-2723, DOI: 10.1039/C4SC00753K.

(108) Fabrication of crystals from single metal atoms, N.P.E. Barry, A. Pitto-Barry, A. M. Sanchez, A.P. Dove, R.J. Procter, J.J. Soldevila-Barreda, N. Kirby, I. Hands-Portman, C.J. Smith, R.K. O'Reilly, R. Beanland, and P.J. Sadler, Nature Commun, 2014, 5, 4851, doi:10.1038/ncomms4851

‡(107) DNA-templated chemistries for sequence controlled oligomer synthesis, P. Milnes, R.K.O'Reilly, ACS Symposium Series, Sequence-Controlled Polymers: Synthesis, Self-Assembly, and Properties, 2014, 1107, Chapter 5, 71-84, DOI: 10.1021/bk-2014-1170.ch005.

‡(106) Functional Degradable Polymers by Xanthate-Mediated Polymerization, G.G. Hedir, C. Bell, N.S. Ieong, E. Chapman, I. Collins, R.K. O'Reilly, A.P. Dove, Macromolecules, 2014, 47, 2847-2852, DOI: 10.1021/ma500428e

‡(105) Precision Polymers: A Kinetic Approach for Functional Poly(norbornenes), D. Moatsou, C.F. Hansell, R.K. O'Reilly, Chem. Sci, 2014, 5, 2246-2250, DOI:10.1039/C4SC00752B

‡(104) Exploiting the tetrazine-norbornene reaction for single polymer chain collapse, C.F. Hansell, A. Lu, J.P. Patterson, R.K. O'Reilly, Nanoscale, 2014, 4102-4107, 6, DOI: 10.1039/C3NR06706H

‡(103) The analysis of solution self-assembled polymeric nanomaterials, J.P. Patterson, M.P. Robin, C.Chassenieux, O. Colombani, R.K.O’Reilly, Chem Soc Rev, 2014, 2412-2425, DOI: 10.1039/C3CS60454C.

‡(102) Studying the activity of the MacMillan catalyst embedded within hydrophobic crosslinked polymeric nanostructures, B. Moore, D. Moatsou, A. Lu, R.K. O'Reilly, Polymer Chemistry, 2014, 3487-3494, DOI:10.1039/C3PY01734F.

‡(101) Construction of DNA–polymer hybrids using intercalation interactions, T. Wilks, A. Pitto-Barry, N. Kirby, E. Stulz, R.K. O'Reilly, Chem Commun, 2014, 50, 1338-1340, DOI:10.1039/C3CC48726A.

‡(100) Expanding the scope of the crystallization-driven self-assembly of polylactide-containing polymers, A. Pitto-Barry, N. Kirby, A. P. Dove, R.K. O'Reilly, Polymer Chemistry, 2014, 5, 1427-1436, DOI: 10.1039/C3PY01048A.

‡(99) One–pot synthesis of responsive sulfobetaine nanoparticles by RAFT polymerisation: the effect of branching on the UCST cloud point, H. Willcock, A. Lu, C.F Hansell, E. Chapman, I. Collins, R.K. O'Reilly, Polymer Chemistry, 2014, 5, 1023-1030, DOI: 10.1039/C3PY00998J.

(98) Glutathione-Triggered Disassembly of Isothermally Responsive Polymer
Nanoparticles obtained by Nanoprecipitation of Hydrophilic Polymers, D. J. Phillips, J. P. Patterson, R. K. O'Reilly and M. I. Gibson, Polymer Chemistry, 2014, 5, 126-131. DOI: 10.1039/C3PY00991B


‡(97) Tuning the Size of Cylindrical Micelles from Poly(L-Lactide)-b-Poly(Acrylic Acid) Diblock Copolymers based on Crystallization-Driven Self-Assembly, L. Sun, N. Petzetakis, A. Pitto-Barry, T. Schiller, N. Kirby, D. Keddie, B. Boyd, R.K. O'Reilly, A.P. Dove, Macromolecules, 2013, 46, 9074–9082. DOI: 10.1021/ma401634s

‡(96) 'Giant Surfactants' Created by the Fast and Efficient Functionalization of a DNA Tetrahedron with a Temperature-Responsive Polymer, T. Wilks, J. Bath, Jan de Vries, J. Raymond, A. Herrmann, A.J. Turberfield, R.K. O'Reilly, ACS Nano, 2013, 7, 8561-8572. DOI:10.1021/nn402642a

(95) Poly(methyl methacrylate-block-vinyl-m-triphenylamine): synthesis by RAFT polymerization and melt-state self-assembly, S. Mastroianni, J.P. Patterson, R.K.O'Reilly, T.H. Epps III, Soft Matter, 2013, 9, 10146 - 10154. DOI:10.1039/C3SM51806J

(94) Advantages of Block Copolymer Synthesis by RAFT-Controlled Dispersion
Polymerization in Supercritical Carbon Dioxide, J. Jennings, M. Beija, J. Kennon, H. Willcock, R.K. O'Reilly, S, Rimmer, S. Howdle, Macromolecules, 2013, 46, 6843-6851. DOI: 10.1021/ma401051e

‡(93) Stimuli Responsive Materials, P. Theato, B. S. Sumerlin, R. K. O'Reilly and T. H. Epps, III Chem. Soc. Rev., 2013, 42, 7055-7056. DOI: 10.1039/C3CS90057F

‡(92) Structural characterization of amphiphilic homopolymer micelles using light scattering, SANS, and cryo-TEM, J. Patterson, E. Kelley, R. Murphy, A. Moughton, M. Robin, A, Lu, O. Colombani, C. Chassenieux, D. Cheung, M. Sullivan, T.H. Epps, III, R.K. O'Reilly, Macromolecules, 2013, 46, 6319-6325. DOI: 10.1021/ma4007544

‡(91) New functional handle for use as a self-reporting contrast and delivery agent in nanomedicine, M. Robin, A.B. Mabire, J. Damborsky, E. Thom, U. Winzer-Serhan, J. Raymond, R.K. O'Reilly, J. Am. Chem. Soc., 2013, 135, 9518–9524. DOI: 10.1021/ja403587c

‡(90) Effect of Complementary Nucleobase Interactions on the Copolymer Composition of RAFT Copolymerizations, Y. Kang, A. Lu, A. Ellington, M.C. Jewett, R.K. O'Reilly, ACS Macro Letters, 2013, 2, 581-586. DOI: 10.1021/mz4001833

‡(89) A Comparative Study of the Stimuli-Responsive Properties of DMAEA and DMAEMA containing polymers, P. Cotanda, D.B. Wright, M. Tyler, R.K. O'Reilly, J. Polym. Sci. Part A: Polym. Chem. 2013, 51, 3333-3338. DOI: 10.1002/pola.26730

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(88) Chemically programmed self-sorting of gelator networks, K. L. Morris, L. Chen, J. Raeburn, O. R. Sellick, P. Cotanda, A. Paul, P. C. Griffiths, S. M. King, R. K. O’Reilly, L. C. Serpell and D. J. Adams, Nature Commun, 2013, 4, 1480. DOI:10.1038/ncomms2499.

(87) Hybrid inorganic-organic composite nanoparticles from crosslinkable polyfluorenes, J. M. Behrendt , A. B Foster , M. McCairn , H. Willcock , R. K. O'Reilly and M. Turner, J. Mater. Chem. C, 2013, 1, 3297-3304. DOI: 10.1039/C3TC30266K.

‡(86) To Aggregate, or not to Aggregate? Considerations in the Design and Application of Polymeric Thermally-Responsive Nanoparticles, M. I. Gibson and R. K. O’Reilly, Chem. Soc. Rev. 2013, 42, 7204-7213, DOI: 10.1039/C3CS60035A.

‡(85) Polymer chemistry: Not lost in translation, R. K. O'Reilly, Nature Chemistry, 2013, 252, DOI:10.1038/nchem.1603.

‡(84) Thermoresponsive polymer-supported L-proline micelle catalysts for the direct asymmetric aldol reaction in water, H.A. Zayas, A. Lu, D. Valade, F. Amir, Z. Jia, R.K.O'Reilly and M. Monterio, ACS Macro Letters, 2013, 2, 327; DOI: 10.1021/mz4000943

(83) A new approach to high resolution, high contrast electron microscopy of macromolecular block copolymer assemblies, M. A. Dyson, A. M. Sanchez, J. P. Patterson, R. K. O’Reilly, J. Sloan and N. R. Wilson, Soft Matter, 2013, 9, 3741-3749. DOI: 10.1039/C3SM27787A

‡(82) Conjugation-Induced Fluorescent Labeling of Proteins and Polymer Using Dithiomaleimides, M. Robin, P. Wilson, A. Mabire, J. Kiviaho, J. Raymond, D.M. Haddleton and R. K. O’Reilly, J. Am. Chem. Soc. 2013, 135, 2875-2878. DOI: 10.1021/ja3105494

‡(81) Hollow Block Copolymer Nanoparticles through a Spontaneous One-Step Structural Reorganization, N. Petzetakis, M. Robin, J.P. Patterson, E. Kelley, P. Cotanda, P.H.H. Bomans, N. Sommerdijk, A.P. Dove, T.H. Epps, III and R.K. O'Reilly, ACS Nano, 2013, 7, 1120 - 1128. DOI: 10.1021/nn400272p

‡(80) Immobilization of MacMillan Catalyst via Controlled Radical Polymerization: Catalytic Activity and Reuse, B. L. Moore, A. Lu, D.A. Longbottom and R. K. O’Reilly, Polymer Chemistry, 2013, 4, 2304 - 2312. DOI: 10.1039/C3PY21125H

‡(79) Catalytic Y-tailed amphiphilic homopolymers – aqueous nanoreactors for high activity, low loading SCS pincer catalysts, J. P. Patterson, P. Cotanda, E. G. Kelley, A. O. Moughton, A. Lu, T. H. Epps, III and R. K. O’Reilly, Polymer Chemistry, 2013, 4, 2033 - 2039. DOI: 10.1039/C3PY21137A

‡(78) Advances in nanoreactor technology using polymeric nanostructures, A. Lu and R.K. O'Reilly, Current Opinion in Biotechnology, 2013, 24, 639-645. DOI: 10.1016/j.copbio.2012.11.013

(77) Fluorescent nanoparticles from PEGylated polyfluorenes, J. M. Behrendt , Y. Wang , H. Willcock , L. Wall , M. C. McCairn, R. K. O'Reilly and M. L. Turner, Polymer Chemistry, 2013. DOI: 10.1039/C3PY21068E

‡(76) Tuning the Catalytic Activity of L-Proline Functionalized Hydrophobic Nanogel Particles in Water, A. Lu, D. Moatsou, D.A. Longbottom and R.K. O'Reilly, Chem. Sci. 2013, 4, 965-969. DOI: 10.1039/C2SC21300A

(75) Mutual binding of polymer end-groups by complementary p-p stacking a molecular "Roman Handshake", B. W. Greenland, M. B. Bird, S. Burattini, R. Cramer, R. K. O’Reilly, J. P. Patterson, W. Hayes, C.J. Cardin and H. M. Colquhoun, Chem. Commun. 2013, 49, 454-456, DOI: 10.1039/c2cc35965k 

Featured on inside front cover


‡(74) Catalytic polymeric nanoreactors: more than a solid supported catalyst, P. Cotanda, N. Petzetakis and R.K. O'Reilly, MRS Communications, 2012, 2, 119-126, DOI: 10.1557/mrc.2012.26

‡(73) Orthogonal Modification of Norbornene-Functional Degradable Polymers, R. J. WIlliams, I. Barker, R.K. O'Reilly and A.P. Dove, ACS Macro Letters 2012, 1285-1290. DOI: 10.1021/mz300496q

‡(72) Molecular recognition driven catalysis using polymeric nanoreactors, P. Cotanda and R.K. O'Reilly, Chem. Commun. 2012, 48, 10280-10282. DOI: 10.1039/C2CC35655D

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‡(71) pH-switchable polymer nanostructures for controlled release, K.E.B. Doncom, C.F. Hansell, P. Theato and R.K. O'Reilly, Polym. Chem., 2012, 3, 3007-3015, DOI: 10.1039/C2PY20545A

(70) Atom Transfer Cyclization with CuSO4 / KBH4: a formal AGET process also
applicable to ATRP, A. J. Clark, A. E. Collis, D. A. Fox, L. Hepple, N. James, J. P. McDonagh, R.K. O’Reilly, H. Parekh, A. Ross, A.B. Sellars, H. Willcock and P. Wilson, J. Org. Chem., 2012, 17, 6778-6788.

VIP article

‡(69) Aldol Reactions Catalyzed by L-Proline Functionalized Polymeric Nanoreactors in Water, A. Lu, P. Cotanda, J. P. Patterson, D. Longbottom and R.K. O'Reilly, Chem. Commun. 2012, 48, 9699-9701, DOI: 10.1039/C2CC35170F

‡(68) Nucleobase Containing Synthetic Polymers: Advancing Biomimicry via Controlled Synthesis and Self-Assembly, R. McHale and R.K. O'Reilly, Macromolecules, 2012, 45, 7665-7675, DOI: 10.021/ma300895u

Perspective artice featured on the front cover

‡(67) A Mix-and-Click Approach to Double Core Shell Micelle Functionalization, C.F. Hansell and R.K.O'Reilly, ACS Macro Letters, 2012, 1, 896-901. DOI: 10.1021/mz300230c

‡(66) Crystallization Driven Sphere-to-rod Transition of Poly(lactide)-b-Poly(acrylic acid) Diblock Copolymers: Mechanism and Kinetics, N. Petzetakis, A.P. Dove, R.K. O'Reilly, Soft Matter, 2012, 8, 7408-7414; DOI: 10.1039/C2SM25247C

‡(65) Preparation of chiral amino acid materials and the study of their interactions with 1'1-bi-2-naphthol, B.L. Moore and R.K. O'Reilly, J. Polym. Sci. Part A, 2012, 50, 3567-3574. DOI: 10.1002/pola.26141

‡(64) Degradable Graft Copolymers by Ring-Opening and Reverse Addition-Fragmentation Chain Transfer Polymerization, R.J. Williams, R. K. O'Reilly and A.P. Dove, Polymer Chem. 2012, 3, 2156-2164, DOI: 10.1039/C2PY20213A

Paper of the week

‡(63) Sequence-specific synthesis of macromolecules using DNA templated chemistry, P. Milnes, M. McKee, J. Bath, E. Stulz, A.J. Turberfield, R.K. O’Reilly, Chem. Commun. 2012, 48, 5614-5616. DOI: 10.1039/C2CC31975F

‡(62) Biomimetic Radical Polymerization via Cooperative Assembly of Segregating Templates, R. McHale, J.P. Patterson, P.B. Zetterlund, R.K. O'Reilly, Nature Chemistry, 2012, 491-497. DOI: 10.1038/nchem.1331

Highlighted in Nature Materials - see the link

(61) Multi-component Organic Nanoparticles for Fluorescent Studies in Biological Systems, T. O. McDonald, P. Martin, J. P. Patterson, D. Smith, M. Giardiello, M. Marcello, V. See, R.K. O’Reilly, A. Owen, S. Rannard, Adv. Funct. Mater. 2012, 22, 2469-2478, DOI: 10.1002/adfm.201103059

‡(60) Functionalized organocatalytic nanoreactors: hydrophobic pockets for acylation reactions in water, P. Cotanda, A. Lu, J. P. Patterson, N. Petzetakis, R. K. O’Reilly, Macromolecules, 2012, 45, 2377, DOI: 10.1021/ma2027462

‡(59) Self-Assembled Nanoparticles, R. K. O'Reilly, Supramolecular Chemistry: from Molecules to Nanomaterials, J.W. Steed and P.A. Gale (Eds). John Wiley & Sons Ltd, Chichester, UK, 2012, 3699-3718.

‡(58) Polymers with molecular weight dependent LCSTs are essential for cooperative behaviour, N. S. Ieong, M. Hasan, D. J. Phillips, Y. Saaka, R.K. O'Reilly, M.I. Gibson, Polym. Chem. 2012, 3, 794-799. DOI: 10.1039/C2PY00604A

(57) Programmable one-pot multistep organic synthesis using DNA junctions, M. McKee, P. Milnes, J. Bath, E. Stulz, R.K. O’Reilly, A.J. Turberfield, J. Am. Chem. Soc. 2012, 134, 1446-1449. DOI: 10.1021/ja2101196

‡(56) Dibromomaleimide end functional polymers by RAFT polymerization without the need of protecting groups, M. Robin, M. Jones, D.M. Haddleton, R.K. O'Reilly, ACS Macro Lett., 2012, 1, 222-226. DOI: 10.1021/mz200164x

‡(55) A simple approach to characterizing block copolymer assemblies: graphene oxide supports for high contrast multi-technique imaging, J.P. Patterson, A. M. Sanchez, N. Petzetakis, T.P. Smart, T. H. Epps III, I. Portman, N. R. Wilson, R.K. O’Reilly, Soft Matter, 2012, 8, 3322-3328. DOI: 10.1039/c2sm07040e

Graphic featured on the front cover.

Press coverage in Materials Today (Impact Factor - 6.265) - see the link


(54) Crystal growth inhibition of tetrahydrofuran hydrate with poly(N-vinyl piperidone) and other poly(N-vinyl lactam) homopolymers, R. O'Reilly, N.S. Ieong, P.C. Chua, M. A. Kelland, Chem. Eng. Sci, 2011, 66, 6555-6560. DOI: 10.1016/j.ces.2011.09.010

(53) The critical importance of size on thermoresponsive nanoparticle transition temperatures: gold and micelle-based polymer nanoparticles, N. S. Ieong, K. Brebis, L. E. Daniel, R. K. O'Reilly and M. I. Gibson, Chem. Commun., 2011, 11627-11629. DOI: 10.1039/C1CC15171A

(52) The missing lactam poly(N-vinyl lactam) kinetic hydrate inhibitor – high pressure kinetic hydrate inhibition of structure II gas hydrates with poly(N-vinyl piperidone) and other poly (N-vinyl lactam) homopolymers, R.K. O’Reilly, N.S. Ieong, P.C. Chua, M. Kelland, Energy and Fuels, 2011, 25, 4595-4599. DOI: 10.1021/ef2009953

‡ (51) L-Proline functionalized polymers prepared by RAFT polymerization and their assemblies as supported organocatalysts, A. Lu, T. P. Smart, T. H. Epps III, D. A. Longbottom, R. K. O’Reilly, Macromolecules, 2011, 44, 7233-7241. DOI: 10.1021/ma201256m

(50) Stereocomplexation in novel degradable amphiphilic block copolymer micelles of poly(ethylene oxide) and poly(benzyl α-malate), R. J. Pounder, H. Willcock, N. S. Ieong, R. K. O’Reilly, A. P. Dove, Soft Matter, 2011, 7, 10987-10993. DOI: 10.1039/c1sm06164j

‡ (49) Additive-free Clicking for Polymer Functionalization and Coupling by Tetrazine-Norbornene Chemistry, C. F. Hansell, P. Espeel, M. M. Stamenovic, I. A. Barker, A. P. Dove, F. E. Du Prez, R. K. O’Reilly, J. Am. Chem. Soc., 2011, 133, 13828-13831. DOI: 10.1021/ja203957h

(48) Tetrazine-Norbornene ‘Click’ Reactions to Functionalize Degradable Polymers Derived from Lactide, I. A. Barker, D. J. Hall, C. F. Hansell, R. K. O’Reilly, A. P. Dove, Macromol. Rapid Commun., 2011, 32, 1362-1366. DOI: 10.1002/marc.201100324.

‡(47) pH-responsive chiral nanostructures, J. Du, H. Willcock, N. S. Ieong, R. K. O'Reilly, Aust. J Chem., 2011, 64, 1041-1046. DOI: 10.1071/CH11131

‡ (46) Self-assembly of Hydrophilic Homopolymers: A Matter of End Groups, J. Du, H. Willcock, J.P. Patterson, R. K. O'Reilly, Small, 2011, 7, 2070-2080. DOI: 10.1002/smll.201100382

Highlighted as Editors' choice Science, July 2011, see link.

(45) Highly active, thermo-responsive polymeric catalytic system for reuse in aqueous and organic CuAAC reactions, M. Lammens, S. Wallyn, R. K. O'Reilly, F. Du Prez, J. Polym. Sci. Part A, Polym. Chem., 2011, 49, 2878-2885. DOI: 10.1002/pola.24723

‡ (44) Cylindrical Micelles of Controlled Length from the Crystallization-Driven Self-Assembly of Poly(lactide)-Containing Block Copolymers, N. Petzetakis, A.P. Dove, R. K. O'Reilly, Chem. Sci., 2011, 2, 955-960. DOI: 10.1039/c0sc00596g

‡ (43) Anisotropic particles with patchy, multicompartment and Janus architecture: preparation and application, J. Du, R. K. O'Reilly, Chem. Soc. Rev., 2011, 40, 2402-2416. DOI: 10.1039/c0cs00216j

‡ (42) The Missing Lactam-Thermoresponsive and Biocompatible Poly(N-vinylpiperidone) Polymers by Xanthate-Mediated RAFT Polymerization, N. S. Ieong, M. Redhead, C. Bosquillon, C. Alexander, M. Kelland, R. K. O'Reilly, Macromolecules., 2011, 44, 886-893. DOI: 10.1021/ma1026466

‡ (41) Exploring RAFT Polymerization for the Synthesis of Bipolar Diblock Copolymers and their Supramolecular Self-Assembly, P. E. Williams, A. O. Moughton, S. Khodabakhsh, J. P. Patterson, R. K. O'Reilly, Polym. Chem., 2011, 2, 720-729. DOI: 10.1039/C0PY00359J

‡ (40) Peptidomimetic bond formation by DNA-templated acyl transfer, E. Stulz, A. J. Turberfield, R. K. O'Reilly, S. R. Gerrard, M. L. McKee and A. C. Evans, Org. Biomol. Chem., 2011,9, 1661-1666. DOI: 10.1039/C0OB00753F

‡ (39) Reversible solution morphology switching nanostructures, A.O. Moughton, J.P. Patterson, R.K. O'Reilly, Chem. Commun., 2011, 47, 355-357. DOI: 10.1039/C0CC02160A
Special issue for world-wide emerging investigators

‡ (38) Functional polymeric nanostructures prepared by self-assembly and beyond, R.K. O'Reilly, Complex Macromolecular Architectures: Synthesis, Characterization and Self Assembly, John Wiley and Sons, 2011, Chapter 17, 527-560. 


(37) Polymeric ligands as homogeneous, reusable catalyst systems for copper assisted click chemistry, M. Lammens, J. Skey, S. Wallyn, R.K. O'Reilly, F. Du Prez, Chem. Commun., 2010, 46, 8719-8721. DOI: 10.1039/C0CC01451F

Graphic featured on the front cover.

‡ (36) Multi-step DNA Templated Reactions for the Synthesis of Functional Sequence Controlled Oligomers, M. McKee, P. Milnes, J. Bath, E. Stulz, A. J. Turberfield, R.K. O'Reilly, Angew. Chem. Int. Ed., 2010, 49, 7948-7951. DOI: 10.1002/anie.201002721

‡ (35) Synthesis and self-assembly of amphiphilic chiral poly(amino acid) star polymers, J. Skey, H. Willcock, M. Lammens, F. Du Prez, R.K. O'Reilly, Macromolecules, 2010, 43, 5949-5955. DOI: 10.1021/ma101019g

‡ (34) Organocatalytic Tuneable Amino Acid Polymers Prepared by Controlled Radical Polymerization, A.C. Evans, A. Lu, C. Ondeck, D.A. Longbottom, R.K. O'Reilly, Macromolecules, 2010, 43, 6374-6380. DOI: 10.1021/ma1008447

‡ (33) Using controlled radical polymerisation techniques for the synthesis of functional polymers containing amino acid moieties, R.K. O'Reilly, Polym. International, 2010, 59, 568-573. DOI: 10.1002/pi.2830

‡ (32) pH resonsive vesicles from a schizophrenic chiral diblock copolymer, J. Du, R.K. O'Reilly, Macromol. Chem. Phys., 2010, 211, 1530-1537. DOI: 10.1002/macp.201000022

‡ (31) Stabilization of amino acid derived diblock copolymer micelles through favorable D:L side chain interactions, J. Skey, C.F. Hansell and R.K. O'Reilly, Macromolecules, 2010, 43, 1309-1318. DOI: 10.1021/ma902356u

‡ (30) End group removal and modification of RAFT polymers, H. Willcock and R.K. O'Reilly, Polym. Chem., 2010, 1, 149-157. DOI: 10.1039/B9PY00340A

‡ (29) Thermally induced micelle to vesicle morphology transition for a charged chain end diblock copolymer, A.O. Moughton and R.K. O'Reilly, Chem. Commun., 2010, 46, 1091-1093. DOI: 10.1039/B922289H

‡ (28) Using metallo-supramolecular block copolymers for the synthesis of higher order nanostructure assemblies, A. O. Moughton and R. K. O’Reilly, Macromol. Rapid Commun., 2010, 31, 37-52. DOI: 10.1002/marc.200900496

‡ (27) Using metal ligand interactions for the synthesis of metallostar polymers, L. Munuera and R. K. O’Reilly, Dalton Trans., 2010, 39, 388-391. DOI: 10.1039/B912319A

‡ (26) Functional and tuneable amino acid polymers prepared by RAFT polymerization, A. C. Evans, J. Skey, M. Wright, W. Qu, C. Ondeck, D. A. Longbottom, R. K. O’Reilly, J. Polym. Sci. Part A, Polym. Chem., 2009, 47, 6814-6826. DOI: 10.1002/pola.23721



‡ (25) Mild and facile synthesis of multifunctional RAFT chain transfer agents, C. F. Hansell and R. K. O’Reilly, Polymers, 2009, 1, 3-15. DOI: 10.3390/polym1010003

‡ (24) Advances in smart and functional polymer vesicles, J. Du and R. K. O’Reilly, Soft Matter, 2009, 5, 3544-3561. DOI: 10.1039/B905635A

‡ (23) Hollow nanostructures from self assembled supramolecular metallo-triblock copolymers, A.O. Moughton, K. Stubenrauch, R. K. O’Reilly, Soft Matter, 2009, 5, 2361-2370. DOI: 10.1039/B818955B


‡ (22) Facile one pot synthesis of a range of reversible addition fragmentation chain transfer (RAFT) agents, J. Skey, R.K. O’Reilly, Chem. Commun., 2008, 35, 4183-4185. DOI: 10.1039/B804260H

‡ (21) Non-covalently connected micelles, nanoparticles and metal functionalized nanocages using supramolecular self-assembly, A.O. Moughton, R.K. O’Reilly, J. Am. Chem. Soc., 2008, 130, 8714-8725. DOI: 10.1021/ja800230k

‡ (20) Synthesis of hollow responsive functional nanocages using a non covalently connected micelle strategy, A.D. Ievins, A.O. Moughton, R.K. O'Reilly, Macromolecules, 2008,41, 3571-3578. DOI: 10.1021/ma800047r

‡ (19) Synthesis of chiral micelles and nanoparticles from amino acid based monomers using RAFT polymerization, J. Skey, R.K. O’Reilly, J. Polym. Sci. Part A, Polym. Chem., 2008, 46, 3690-3702. DOI: 10.1002/pola.22710

‡ (18) Synthesis of core functionalized polymer micelles and shell cross-linked nanoparticles, A.D. Ievins, X.S. Wang, A.O. Moughton, J. Skey, R.K.O’Reilly, Macromolecules, 2008, 41, 2998-3006. DOI: 10.1021/ma702702j



‡ (17) Spherical cross-linked polymer micelles: nanosized reaction vessels? R.K. O’Reilly, Phil. Trans. R. Soc. A, 2007, 365, 2863-2878. DOI: 10.1098/rsta.2007.0019

(16) Diimine, diamine, and diphosphine iron catalysts for the controlled radical polymerization of styrene and acrylate monomers, R.K. O’Reilly, M.P. Shaver, V.C. Gibson, Macromolecules, 2007, 40, 7441-7452. DOI: 10.1021/ma070756j

(15) Preparation of orthogonally-functionalized core Click cross-linked nanoparticles, R.K. O'Reilly, M.J. Joralemon, C.J. Hawker, K.L. Wooley, New J. Chem., 2007, 31, 718-724. DOI: 10.1039/B616103K

(14) Where is nano taking us? J. Baumberg, L. Cronin, M. Gee, M. Kearnes, P. MacNaghten, H. Makatsoris, J. Ramsden, R. O’Reilly, M. Webb, Nanotech. Percept., 2007, 3, 3-14.



‡ (13) Cross linked block copolymer micelles: Functional nanostructures of great potential and versatility, R.K. O'Reilly, C.J. Hawker, K.L. Wooley, Chem. Soc. Rev., 2006, 11, 1068-1083. DOI: 10.1039/B514858H

(12) Nickel(II) α-diimine catalysts for the atom transfer radical polymerization of styrene, R. K. O’Reilly, M. P. Shaver, V. C. Gibson, Inorg. Chim. Acta, 2006, 359, 4417-4420. DOI: 10.1016/j.ica.2006.06.026

(11) Fluorogenic 1,3 dipolar addition within the hydrophobic core of a shell cross-linked nanoparticle, R.K. O'Reilly, M.J. Joralemon, C.J. Hawker, K.L. Wooley, Chem. Eur. J., 2006, 12, 6776-6786. DOI: 10.1002/chem.200600467

(10) Facile synthesis of surface-functionalized micelles and shell cross-linked nanoparticles, R.K. O'Reilly, M.J. Joralemon, C.J. Hawker, K.L. Wooley, J. Polym. Sci. Part A, Polym. Chem., 2006, 44, 5203-5217. DOI: 10.1002/pola.21602



(9) Shell Click-crosslinked (SCC) Nanoparticles: A New Methodology for Synthesis and Orthogonal Functionalization, M.J. Joralemon, R.K. O'Reilly, C.J. Hawker, K.L. Wooley, J. Am. Chem. Soc., 2005, 127, 16892-16899. DOI: 10.1021/ja053919x

(8) Functionalization of micelles and shell cross-linked nanoparticles using Click chemistry, R.K. O'Reilly, M.J. Joralemon, C.J. Hawker, K.L. Wooley, Chem. Mater., 2005, 17, 5976-5988. DOI: 10.1021/cm051047s

(7) Dendrimers Clicked Together Divergently, M.J. Joralemon, R.K. O'Reilly, J.B. Matson, A.K. Nugent, C.J. Hawker, K.L. Wooley, Macromolecules, 2005, 38, 5436-5443. DOI: 10.1021/ma050302r

(6) Five-coordinate iron(II) complexes bearing tridentate nitrogen donor ligands as catalysts for atom transfer radical polymerisation, V.C. Gibson, R.K. O’Reilly, A.J.P. White, D.J. Williams, Polyhedron, 2004, 23, 2921-2928. DOI: 10.1016/j.poly.2004.09.001

(5) Design of highly active iron-based catalysts for Atom Transfer Radical Polymerization: Tridentate salicylaldiminato ligands affording near ideal Nernstian Behavior, V.C. Gibson, R.K. O’Reilly, A.J.P. White, D.J. Williams, J. Am. Chem. Soc., 2003, 125, 8450-8451. DOI: 10.1021/ja035458q

(4) Iron complexes bearing iminopyridine and aminopyridine ligands as catalysts for Atom Transfer Radical Polymerisation, V.C. Gibson, R.K. O’Reilly, D.F. Wass, A.J.P. White, D.J. Williams, J. Chem. Soc., Dalton Trans., 2003, 2824-2830. DOI: 10.1039/B303094F

(3) Polymerisation of Methyl Methacrylate using four-coordinate (a-diimine) iron catalysts: Atom Transfer Radical Polymerization versus Catalytic Chain Transfer, V.C. Gibson, R.K. O’Reilly, D.F. Wass, A.J.P. White, D.J. Williams, Macromolecules, 2003, 36, 2591-2593. DOI: 10.1021/ma034046z

(2) Four coordinate iron complexes bearing a-diimine ligands: efficient catalysts for Atom Transfer Radical Polymerisation, V.C. Gibson, R.K. O’Reilly, W. Reed, D.F. Wass, A.J.P. White, D.J. Williams, Chem. Commun., 2002, 17, 1850-1851. DOI: 10.1039/B204510A

(1) Reactivity and Characterisation of Transition-Metal Carbonyl Clusters using UV Laser Desorption Mass Spectrometry, G. Critchley, P.J. Dyson, B.F.G. Johnson, J.S. McIndoe, R.K. O'Reilly, P.R.R. Langridge-Smith, Organometallics, 1999, 18, 4090-4097. DOI: 10.1021/om990075f


‡indicates that Prof O’Reilly is the corresponding author