| Photo-reversible dimerisation reactions and their applications in polymeric systems G Kaur, P Johnston, K Saito Polymer Chemistry 5 (7), 2171-2186, 2014 | 214 | 2014 |
| Synthesis, properties and performance of organic polymers employed in flocculation applications VH Dao, NR Cameron, K Saito Polymer Chemistry 7 (1), 11-25, 2016 | 167 | 2016 |
| Synthesis of a diamine cross-linker containing Diels–Alder adducts to produce self-healing thermosetting epoxy polymer from a widely used epoxy monomer N Bai, K Saito, GP Simon Polymer Chemistry 4 (3), 724-730, 2013 | 156 | 2013 |
| Recent developments in chemical degradation of lignin: catalytic oxidation and ionic liquids J Dai, AF Patti, K Saito Tetrahedron Letters 57 (45), 4945-4951, 2016 | 111 | 2016 |
| Chemical depolymerization of lignin involving the redistribution mechanism with phenols and repolymerization of depolymerized products S Nanayakkara, AF Patti, K Saito Green Chemistry 16 (4), 1897-1903, 2014 | 90 | 2014 |
| Importance of mediators for lignin degradation by fungal laccase LF Longe, J Couvreur, M Leriche Grandchamp, G Garnier, F Allais, ... ACS sustainable chemistry & engineering 6 (8), 10097-10107, 2018 | 89 | 2018 |
| Strategic approach towards plastic waste valorization: challenges and promising chemical upcycling possibilities PS Roy, G Garnier, F Allais, K Saito ChemSusChem 14 (19), 4007-4027, 2021 | 86 | 2021 |
| Oxidative polymerization of 2, 6-dimethylphenol to form poly (2, 6-dimethyl-1, 4-phenyleneoxide) in water K Saito, T Tago, T Masuyama, H Nishide Angewandte Chemie-International Edition 43 (6), 730-733, 2004 | 81 | 2004 |
| Are lignin-derived monomers and polymers truly sustainable? An in-depth green metrics calculations approach S Fadlallah, PS Roy, G Garnier, K Saito, F Allais Green Chemistry 23 (4), 1495-1535, 2021 | 76 | 2021 |
| Lignin depolymerization with phenol via redistribution mechanism in ionic liquids S Nanayakkara, AF Patti, K Saito ACS Sustainable Chemistry & Engineering 2 (9), 2159-2164, 2014 | 67 | 2014 |
| Synthesis and characterization of chitosan modified polyurethane bio-nanocomposites with biomedical potential MA Javaid, RA Khera, KM Zia, K Saito, IA Bhatti, M Asghar International journal of biological macromolecules 115, 375-384, 2018 | 60 | 2018 |
| Topochemical photo-reversible polymerization of a bioinspired monomer and its recovery and repolymerization after photo-depolymerization P Johnston, C Braybrook, K Saito Chemical Science 3 (7), 2301-2306, 2012 | 59 | 2012 |
| Photoreversible smart polymers based on 2π+ 2π cycloaddition reactions: nanofilms to self-healing films M Abdallh, C Yoshikawa, MTW Hearn, GP Simon, K Saito Macromolecules 52 (6), 2446-2455, 2019 | 53 | 2019 |
| Light triggered self-healing of polyacrylate polymers crosslinked with 7-methacryloyoxycoumarin crosslinker M Abdallh, MTW Hearn, GP Simon, K Saito Polymer Chemistry 8 (38), 5875-5883, 2017 | 52 | 2017 |
| Thermal degradation behavior and X-ray diffraction studies of chitosan based polyurethane bio-nanocomposites using different diisocyanates MA Javaid, M Rizwan, RA Khera, KM Zia, K Saito, M Zuber, J Iqbal, ... International journal of biological macromolecules 117, 762-772, 2018 | 51 | 2018 |
| Light-healable epoxy polymer networks via anthracene dimer scission of diamine crosslinker T Hughes, GP Simon, K Saito ACS applied materials & interfaces 11 (21), 19429-19443, 2019 | 49 | 2019 |
| Stimuli-responsive polymeric materials for separation of biomolecules S Tan, K Saito, MTW Hearn Current opinion in biotechnology 53, 209-223, 2018 | 48 | 2018 |
| TEMPO radical polymer grafted silicas as solid state catalysts for the oxidation of alcohols K Saito, K Hirose, T Okayasu, H Nishide, MTW Hearn RSC advances 3 (25), 9752-9756, 2013 | 48 | 2013 |
| Investigation of the thermal self-healing mechanism in a cross-linked epoxy system N Bai, GP Simon, K Saito RSC advances 3 (43), 20699-20707, 2013 | 48 | 2013 |
| First synthesis of high molecular weight poly (2, 6-difluoro-1, 4-phenylene oxide) by oxidative polymerization K Oyaizu, Y Kumaki, K Saito, E Tsuchida Macromolecules 33 (16), 5766-5769, 2000 | 48 | 2000 |
