BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Lava K, Verbraeken B, Hoogenboom R. Poly(2-oxazoline)s and click chemistry: A versatile toolbox toward multi-functional polymers. European Polymer Journal 2015;65:98-111. [DOI: 10.1016/j.eurpolymj.2015.01.014] [Cited by in Crossref: 113] [Cited by in F6Publishing: 113] [Article Influence: 14.1] [Reference Citation Analysis]
Number Citing Articles
1 Yao X, Qi C, Sun C, Huo F, Jiang X. Poly(ethylene glycol) alternatives in biomedical applications. Nano Today 2023;48:101738. [DOI: 10.1016/j.nantod.2022.101738] [Reference Citation Analysis]
2 Gubarev AS, Lezov AA, Podsevalnikova AN, Mikusheva NG, Fetin PA, Zorin IM, Aseyev VO, Sedlacek O, Hoogenboom R, Tsvetkov NV. Conformational Parameters and Hydrodynamic Behavior of Poly(2-Methyl-2-Oxazoline) in a Broad Molar Mass Range. Polymers 2023;15:623. [DOI: 10.3390/polym15030623] [Reference Citation Analysis]
3 Leiske MN. Poly(2-oxazoline)-derived star-shaped polymers as potential materials for biomedical applications: A review. European Polymer Journal 2023. [DOI: 10.1016/j.eurpolymj.2023.111832] [Reference Citation Analysis]
4 Hayes G, Drain B, Lefley J, Becer CR. Hybrid Multiblock Copolymers of 2-Oxazoline and Acrylates via Cu-Catalyzed Azide–Alkyne Cycloaddition Step-Growth Mechanism. Macromolecules 2022. [DOI: 10.1021/acs.macromol.2c01865] [Reference Citation Analysis]
5 Lusina A, Nazim T, Cegłowski M. Poly(2-oxazoline)s as Stimuli-Responsive Materials for Biomedical Applications: Recent Developments of Polish Scientists. Polymers (Basel) 2022;14:4176. [PMID: 36236124 DOI: 10.3390/polym14194176] [Reference Citation Analysis]
6 Nemati Mahand S, Aliakbarzadeh S, Moghaddam A, Salehi Moghaddam A, Kruppke B, Nasrollahzadeh M, Khonakdar HA. Polyoxazoline: A review article from polymerization to smart behaviors and biomedical applications. European Polymer Journal 2022;178:111484. [DOI: 10.1016/j.eurpolymj.2022.111484] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
7 Rengifo J, Zschoche S, Voit B, Carlos Rueda J. Synthesis and characterization of new interpenetrated hydrogels from N-isopropylacrylamide, 2-oxazoline macromonomer and acrylamide. European Polymer Journal 2022;177:111456. [DOI: 10.1016/j.eurpolymj.2022.111456] [Reference Citation Analysis]
8 Onugwu AL, Attama AA, Nnamani PO, Onugwu SO, Onuigbo EB, Khutoryanskiy VV. Development and optimization of solid lipid nanoparticles coated with chitosan and poly(2-ethyl-2-oxazoline) for ocular drug delivery of ciprofloxacin. Journal of Drug Delivery Science and Technology 2022;74:103527. [DOI: 10.1016/j.jddst.2022.103527] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
9 Gao YZ, Li A, Chen JC, Cui Z, Wu YX. Quaternized Sodium Alginate-g-Ethyl-Oxazoline Copolymer Brushes and Their Supramolecular Networks via Hydrogen Bonding. ACS Biomater Sci Eng 2022. [PMID: 35878006 DOI: 10.1021/acsbiomaterials.2c00436] [Reference Citation Analysis]
10 Wu K, Zhang S, Liu Q, Xu P, Zhang J, Wang D, Zhuo L, Jian X. Poly(arylene ether sulfone) containing diphenyl-biphthalazin-dione moieties with excellent thermal resistance. Polymer 2022. [DOI: 10.1016/j.polymer.2022.124653] [Reference Citation Analysis]
11 Arraez FJ, Xu X, Edeleva M, Van Steenberge PHM, Marien YW, Jerca V, Hoogenboom R, D'hooge DR. Differences and similarities between mono-, bi- or tetrafunctional initiated cationic ring-opening polymerization of 2-oxazolines. Polym Chem . [DOI: 10.1039/d1py01471d] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Mazrad ZAI, Lai M, Davis TP, Nicolazzo JA, Thurecht KJ, Leiske MN, Kempe K. Protected amine-functional initiators for the synthesis of α-amine homo- and heterotelechelic poly(2-ethyl-2-oxazoline)s. Polym Chem 2022;13:4436-45. [DOI: 10.1039/d2py00649a] [Reference Citation Analysis]
13 Tarannum S, Chauhan N, Ghorai MK. Aziridines and 2H-Azirines: Monocyclic. Comprehensive Heterocyclic Chemistry IV 2022. [DOI: 10.1016/b978-0-12-409547-2.14954-6] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
14 Liu S, Kobayashi S, Nishimura S, Ueda T, Tanaka M. Effect of pendant groups on the blood compatibility and hydration states of poly(2‐oxazoline)s. Journal of Polymer Science 2021;59:2559-70. [DOI: 10.1002/pol.20210410] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
15 Drain BA, Beyer VP, Cattoz B, Becer CR. Solvent Dependency in the Synthesis of Multiblock and Cyclic Poly(2-oxazoline)s. Macromolecules 2021;54:5549-56. [DOI: 10.1021/acs.macromol.1c00529] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
16 Qu P, Kuepfert M, Hashmi M, Weck M. Compartmentalization and Photoregulating Pathways for Incompatible Tandem Catalysis. J Am Chem Soc 2021;143:4705-13. [PMID: 33724020 DOI: 10.1021/jacs.1c00257] [Cited by in Crossref: 21] [Cited by in F6Publishing: 23] [Article Influence: 10.5] [Reference Citation Analysis]
17 Shiri P, Amani AM. A brief overview of catalytic applications of dendrimers containing 1,4-disubstituted-1,2,3-triazoles. Monatsh Chem 2021;152:367-85. [DOI: 10.1007/s00706-021-02753-3] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
18 Gil Alvaradejo G, Glassner M, Kumar R, Trouillet V, Welle A, Wang Y, de la Rosa VR, Sekula-Neuner S, Hirtz M, Hoogenboom R, Delaittre G. Thioacetate-Based Initiators for the Synthesis of Thiol-End-Functionalized Poly(2-oxazoline)s. Macromol Rapid Commun 2020;41:e2000320. [PMID: 33463837 DOI: 10.1002/marc.202000320] [Reference Citation Analysis]
19 Liu Q, Zhang S, Wang Z, Li N, Chen Y, Xu P, Jian X. Poly(aryl ether ketone ketone)s containing diphenyl-biphthalazin-dione moieties with excellent thermo-mechanical performance and solubility. European Polymer Journal 2021;143:110205. [DOI: 10.1016/j.eurpolymj.2020.110205] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
20 Menezes RNLD, Felisberti MI. Combining CROP and ATRP to synthesize pH-responsive poly(2-ethyl-2-oxazoline- b -4-vinylpyridine) block copolymers. Polym Chem 2021;12:4680-95. [DOI: 10.1039/d1py00730k] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
21 Zhao T, Drain B, Yilmaz G, Becer CR. One-pot synthesis of amphiphilic multiblock poly(2-oxazoline)s via para-fluoro-thiol click reactions. Polym Chem 2021;12:6392-6403. [DOI: 10.1039/d1py00944c] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
22 Van Guyse JFR, Bernhard Y, Hoogenboom R. Stoichiometric Control over Partial Transesterification of Polyacrylate Homopolymers as Platform for Functional Copolyacrylates. Macromol Rapid Commun 2020;41:e2000365. [PMID: 32808369 DOI: 10.1002/marc.202000365] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
23 Schoolaert E, Merckx R, Becelaere J, Everaerts M, Van Guyse JFR, Sedlacek O, De Geest BG, Van den Mooter G, D’hooge DR, De Clerck K, Hoogenboom R. Immiscibility of Chemically Alike Amorphous Polymers: Phase Separation of Poly(2-ethyl-2-oxazoline) and Poly(2- n -propyl-2-oxazoline). Macromolecules 2020;53:7590-600. [DOI: 10.1021/acs.macromol.0c00970] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
24 Wilts EM, Long TE. Thiol–ene addition enables tailored synthesis of poly(2‐oxazoline)‐ graft ‐poly(vinyl pyrrolidone) copolymers for binder jetting 3D printing. Polym Int 2020;69:902-11. [DOI: 10.1002/pi.6074] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
25 Schoolaert E, Cossu L, Becelaere J, Van Guyse JF, Tigrine A, Vergaelen M, Hoogenboom R, De Clerck K. Nanofibers with a tunable wettability by electrospinning and physical crosslinking of poly(2-n-propyl-2-oxazoline). Materials & Design 2020;192:108747. [DOI: 10.1016/j.matdes.2020.108747] [Cited by in Crossref: 19] [Cited by in F6Publishing: 14] [Article Influence: 6.3] [Reference Citation Analysis]
26 Delecourt G, Plet L, Bennevault V, Guégan P. Synthesis of Double Hydrophilic Block Copolymers Poly(2-oxazoline- b -ethylenimine) in a Two-Step Procedure. ACS Appl Polym Mater 2020;2:2696-705. [DOI: 10.1021/acsapm.0c00308] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
27 Kirila T, Smirnova A, Kurlykin M, Tenkovtsev A, Filippov A. Self-organization in aqueous solutions of thermosensitive star-shaped and linear gradient copolymers of 2-ethyl-2-oxazoline and 2-isopropyl-2-oxazoline. Colloid Polym Sci 2020;298:535-46. [DOI: 10.1007/s00396-020-04638-z] [Cited by in Crossref: 11] [Cited by in F6Publishing: 2] [Article Influence: 3.7] [Reference Citation Analysis]
28 Pertici V, Trimaille T, Gigmes D. Inputs of Macromolecular Engineering in the Design of Injectable Hydrogels Based on Synthetic Thermoresponsive Polymers. Macromolecules 2020;53:682-92. [DOI: 10.1021/acs.macromol.9b00705] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 4.7] [Reference Citation Analysis]
29 Oleszko-torbus N, Utrata-wesołek A, Bochenek M, Lipowska-kur D, Dworak A, Wałach W. Thermal and crystalline properties of poly(2-oxazoline)s. Polym Chem 2020;11:15-33. [DOI: 10.1039/c9py01316d] [Cited by in Crossref: 16] [Cited by in F6Publishing: 20] [Article Influence: 5.3] [Reference Citation Analysis]
30 Sedlacek O, de la Rosa VR, Hoogenboom R. Poly(2-oxazoline)–protein conjugates. Polymer-Protein Conjugates 2020. [DOI: 10.1016/b978-0-444-64081-9.00018-8] [Reference Citation Analysis]
31 Sedlacek O, Hoogenboom R. Drug Delivery Systems Based on Poly(2‐Oxazoline)s and Poly(2‐Oxazine)s. Adv Therap 2020;3:1900168. [DOI: 10.1002/adtp.201900168] [Cited by in Crossref: 50] [Cited by in F6Publishing: 50] [Article Influence: 12.5] [Reference Citation Analysis]
32 Pizzi D, Humphries J, Morrow JP, Fletcher NL, Bell CA, Thurecht KJ, Kempe K. Poly(2-oxazoline) macromonomers as building blocks for functional and biocompatible polymer architectures. European Polymer Journal 2019;121:109258. [DOI: 10.1016/j.eurpolymj.2019.109258] [Cited by in Crossref: 30] [Cited by in F6Publishing: 29] [Article Influence: 7.5] [Reference Citation Analysis]
33 Delaittre G. Telechelic poly(2-oxazoline)s. European Polymer Journal 2019;121:109281. [DOI: 10.1016/j.eurpolymj.2019.109281] [Cited by in Crossref: 27] [Cited by in F6Publishing: 28] [Article Influence: 6.8] [Reference Citation Analysis]
34 Sedlacek O, de la Rosa VR, Hoogenboom R. Poly(2-oxazoline)-protein conjugates. European Polymer Journal 2019;120:109246. [DOI: 10.1016/j.eurpolymj.2019.109246] [Cited by in Crossref: 23] [Cited by in F6Publishing: 24] [Article Influence: 5.8] [Reference Citation Analysis]
35 Park J, Van Guyse JF, Podevyn A, Bolle EC, Bock N, Linde E, Celina M, Hoogenboom R, Dargaville TR. Influence of side-chain length on long-term release kinetics from poly(2-oxazoline)-drug conjugate networks. European Polymer Journal 2019;120:109217. [DOI: 10.1016/j.eurpolymj.2019.109217] [Cited by in Crossref: 14] [Cited by in F6Publishing: 16] [Article Influence: 3.5] [Reference Citation Analysis]
36 Podevyn A, Arys K, de la Rosa VR, Glassner M, Hoogenboom R. End-group functionalization of poly(2-oxazoline)s using methyl bromoacetate as initiator followed by direct amidation. European Polymer Journal 2019;120:109273. [DOI: 10.1016/j.eurpolymj.2019.109273] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 1.5] [Reference Citation Analysis]
37 Drain BA, Becer CR. Synthetic approaches on conjugation of poly(2-oxazoline)s with vinyl based polymers. European Polymer Journal 2019;119:344-51. [DOI: 10.1016/j.eurpolymj.2019.07.047] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 5.5] [Reference Citation Analysis]
38 Al‐bataineh SA, Cavallaro AA, Michelmore A, Macgregor MN, Whittle JD, Vasilev K. Deposition of 2‐oxazoline‐based plasma polymer coatings using atmospheric pressure helium plasma jet. Plasma Process Polym 2019;16:1900104. [DOI: 10.1002/ppap.201900104] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 2.3] [Reference Citation Analysis]
39 Van Guyse JFR, Verjans J, Vandewalle S, De Bruycker K, Du Prez FE, Hoogenboom R. Full and Partial Amidation of Poly(methyl acrylate) as Basis for Functional Polyacrylamide (Co)Polymers. Macromolecules 2019;52:5102-9. [DOI: 10.1021/acs.macromol.9b00399] [Cited by in Crossref: 19] [Cited by in F6Publishing: 21] [Article Influence: 4.8] [Reference Citation Analysis]
40 Arraez FJ, Xu X, Van Steenberge PHM, Jerca V, Hoogenboom R, D’hooge DR. Macropropagation Rate Coefficients and Branching Levels in Cationic Ring-Opening Polymerization of 2-Ethyl-2-oxazoline through Prediction of Size Exclusion Chromatography Data. Macromolecules 2019;52:4067-78. [DOI: 10.1021/acs.macromol.9b00544] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 3.5] [Reference Citation Analysis]
41 Roy M, Wilsens CHRM, Leoné N, Rastogi S. Use of Bis(pyrrolidone)-Based Dicarboxylic Acids in Poly(ester–amide)-Based Thermosets: Synthesis, Characterization, and Potential Route for Their Chemical Recycling. ACS Sustainable Chem Eng 2019;7:8842-52. [DOI: 10.1021/acssuschemeng.9b00850] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
42 Sahn M, Weber C, Schubert US. Poly(2-oxazoline)-Containing Triblock Copolymers: Synthesis and Applications. Polymer Reviews 2019;59:240-79. [DOI: 10.1080/15583724.2018.1496930] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
43 Van Guyse JFR, Mees MA, Vergaelen M, Baert M, Verbraeken B, Martens PJ, Hoogenboom R. Amidation of methyl ester side chain bearing poly(2-oxazoline)s with tyramine: a quest for a selective and quantitative approach. Polym Chem 2019;10:954-62. [DOI: 10.1039/c9py00014c] [Cited by in Crossref: 23] [Cited by in F6Publishing: 23] [Article Influence: 5.8] [Reference Citation Analysis]
44 Verbraeken B, Hullaert J, van Guyse J, Van Hecke K, Winne J, Hoogenboom R. The Elusive Seven-Membered Cyclic Imino Ether Tetrahydrooxazepine. J Am Chem Soc 2018;140:17404-8. [DOI: 10.1021/jacs.8b10918] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 3.4] [Reference Citation Analysis]
45 Zhou Y, Wu P. Block length-dependent phase transition of poly(N-isopropylacrylamide)-b-poly(2-isopropyl-2-oxazoline) diblock copolymer in water. Polymer 2018;153:250-61. [DOI: 10.1016/j.polymer.2018.08.027] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [Reference Citation Analysis]
46 Kara A, Ozturk N, Esendagli G, Ozkose UU, Gulyuz S, Yilmaz O, Telci D, Bozkir A, Vural I. Development of novel self-assembled polymeric micelles from partially hydrolysed poly(2-ethyl-2-oxazoline)- co -PEI-b-PCL block copolymer as non-viral vectors for plasmid DNA in vitro transfection. Artificial Cells, Nanomedicine, and Biotechnology 2018;46:S264-73. [DOI: 10.1080/21691401.2018.1491478] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 2.4] [Reference Citation Analysis]
47 Pröll C, Nuyken O. Telechelic Polymers. Encyclopedia of Polymer Science and Technology 2018. [DOI: 10.1002/0471440264.pst499.pub2] [Reference Citation Analysis]
48 Verbraeken B, Monnery BD, Lava K, Hoogenboom R. The Chemistry of Poly(2-oxazoline)s. Encyclopedia of Polymer Science and Technology 2018. [DOI: 10.1002/0471440264.pst626.pub2] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
49 Mansfield ED, de la Rosa VR, Kowalczyk RM, Grillo I, Hoogenboom R, Sillence K, Hole P, Williams AC, Khutoryanskiy VV. Side chain variations radically alter the diffusion of poly(2-alkyl-2-oxazoline) functionalised nanoparticles through a mucosal barrier. Biomater Sci 2016;4:1318-27. [PMID: 27400181 DOI: 10.1039/c6bm00375c] [Cited by in Crossref: 52] [Cited by in F6Publishing: 52] [Article Influence: 10.4] [Reference Citation Analysis]
50 Ali MW, Gao Y, Siddiq M, Ye X. A Novel Initiator Containing Alkyne Group for the Polymerization of 2-Ethyl-2-oxazoline. Chinese Journal of Chemical Physics 2018;31:77-84. [DOI: 10.1063/1674-0068/31/cjcp1709171] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
51 Riabtseva A, Kaberov LI, Noirez L, Ryukhtin V, Nardin C, Verbraeken B, Hoogenboom R, Stepanek P, Filippov SK. Structural characterization of nanoparticles formed by fluorinated poly(2-oxazoline)-based polyphiles. European Polymer Journal 2018;99:518-27. [DOI: 10.1016/j.eurpolymj.2018.01.007] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 1.8] [Reference Citation Analysis]
52 Gil Alvaradejo G, Glassner M, Hoogenboom R, Delaittre G. Maleimide end-functionalized poly(2-oxazoline)s by the functional initiator route: synthesis and (bio)conjugation. RSC Adv 2018;8:9471-9. [DOI: 10.1039/c8ra00948a] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 3.2] [Reference Citation Analysis]
53 Abbina S, Parambath A. PEGylation and its alternatives. Engineering of Biomaterials for Drug Delivery Systems 2018. [DOI: 10.1016/b978-0-08-101750-0.00014-3] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 2.6] [Reference Citation Analysis]
54 Nam J, Jung Y, Joe J, Jang W. Dual stimuli-responsive viologen-containing poly(2-isopropyl-2-oxazoline) and its multi-modal electrochromic phase transition. Polym Chem 2018;9:3662-6. [DOI: 10.1039/c8py00591e] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 3.2] [Reference Citation Analysis]
55 Raveendran R, Mullen KM, Wellard RM, Sharma CP, Hoogenboom R, Dargaville TR. Poly(2-oxazoline) block copolymer nanoparticles for curcumin loading and delivery to cancer cells. European Polymer Journal 2017;93:682-94. [DOI: 10.1016/j.eurpolymj.2017.02.043] [Cited by in Crossref: 30] [Cited by in F6Publishing: 26] [Article Influence: 5.0] [Reference Citation Analysis]
56 Moreadith RW, Viegas TX. Poly(2-Oxazoline) Polymers - Synthesis, Characterization, and Applications in Development of POZ Therapeutics. In: Scholz C, editor. Polymers for Biomedicine. Hoboken: John Wiley & Sons, Inc.; 2017. pp. 51-75. [DOI: 10.1002/9781118967904.ch3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
57 Lunn DJ, Discekici EH, Read de Alaniz J, Gutekunst WR, Hawker CJ. Established and emerging strategies for polymer chain-end modification. J Polym Sci Part A: Polym Chem 2017;55:2903-14. [DOI: 10.1002/pola.28575] [Cited by in Crossref: 65] [Cited by in F6Publishing: 65] [Article Influence: 10.8] [Reference Citation Analysis]
58 Kempe K. Chain and Step Growth Polymerizations of Cyclic Imino Ethers: From Poly(2‐oxazoline)s to Poly(ester amide)s. Macromol Chem Phys 2017;218:1700021. [DOI: 10.1002/macp.201700021] [Cited by in Crossref: 32] [Cited by in F6Publishing: 32] [Article Influence: 5.3] [Reference Citation Analysis]
59 Morgese G, Shirmardi shaghasemi B, Causin V, Zenobi-wong M, Ramakrishna SN, Reimhult E, Benetti EM. Next-Generation Polymer Shells for Inorganic Nanoparticles are Highly Compact, Ultra-Dense, and Long-Lasting Cyclic Brushes. Angew Chem 2017;129:4578-82. [DOI: 10.1002/ange.201700196] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 2.0] [Reference Citation Analysis]
60 Morgese G, Shirmardi shaghasemi B, Causin V, Zenobi-wong M, Ramakrishna SN, Reimhult E, Benetti EM. Next-Generation Polymer Shells for Inorganic Nanoparticles are Highly Compact, Ultra-Dense, and Long-Lasting Cyclic Brushes. Angew Chem Int Ed 2017;56:4507-11. [DOI: 10.1002/anie.201700196] [Cited by in Crossref: 74] [Cited by in F6Publishing: 75] [Article Influence: 12.3] [Reference Citation Analysis]
61 Rasolonjatovo B, Pitard B, Haudebourg T, Bennevault V, Guégan P. Synthesis of tetraarm star block copolymer based on polytetrahydrofuran and poly(2-methyl-2-oxazoline) for gene delivery applications. European Polymer Journal 2017;88:689-700. [DOI: 10.1016/j.eurpolymj.2016.09.042] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 2.8] [Reference Citation Analysis]
62 Wilson P, Ke PC, Davis TP, Kempe K. Poly(2-oxazoline)-based micro- and nanoparticles: A review. European Polymer Journal 2017;88:486-515. [DOI: 10.1016/j.eurpolymj.2016.09.011] [Cited by in Crossref: 78] [Cited by in F6Publishing: 79] [Article Influence: 13.0] [Reference Citation Analysis]
63 Osawa S, Ishii T, Takemoto H, Osada K, Kataoka K. A facile amino-functionalization of poly(2-oxazoline)s’ distal end through sequential azido end-capping and Staudinger reactions. European Polymer Journal 2017;88:553-61. [DOI: 10.1016/j.eurpolymj.2016.11.029] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 1.8] [Reference Citation Analysis]
64 Verbraeken B, Monnery BD, Lava K, Hoogenboom R. The chemistry of poly(2-oxazoline)s. European Polymer Journal 2017;88:451-69. [DOI: 10.1016/j.eurpolymj.2016.11.016] [Cited by in Crossref: 171] [Cited by in F6Publishing: 174] [Article Influence: 28.5] [Reference Citation Analysis]
65 Kaberov LI, Verbraeken B, Hruby M, Riabtseva A, Kovacik L, Kereïche S, Brus J, Stepanek P, Hoogenboom R, Filippov SK. Novel triphilic block copolymers based on poly(2-methyl-2-oxazoline)–block–poly(2-octyl-2-oxazoline) with different terminal perfluoroalkyl fragments: Synthesis and self-assembly behaviour. European Polymer Journal 2017;88:645-55. [DOI: 10.1016/j.eurpolymj.2016.10.016] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 2.8] [Reference Citation Analysis]
66 Ozkose UU, Altinkok C, Yilmaz O, Alpturk O, Tasdelen MA. In-situ preparation of poly(2-ethyl-2-oxazoline)/clay nanocomposites via living cationic ring-opening polymerization. European Polymer Journal 2017;88:586-93. [DOI: 10.1016/j.eurpolymj.2016.07.004] [Cited by in Crossref: 25] [Cited by in F6Publishing: 25] [Article Influence: 4.2] [Reference Citation Analysis]
67 Kosakowska KA, Dimitrov P, Panambur G, Grayson SM. MALDI-TOF MS investigation of the unconventional termination of living polyoxazoline with ammonia. J Polym Sci Part A: Polym Chem 2017;55:1303-12. [DOI: 10.1002/pola.28495] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
68 England RM, Hare JI, Barnes J, Wilson J, Smith A, Strittmatter N, Kemmitt PD, Waring MJ, Barry ST, Alexander C, Ashford MB. Tumour regression and improved gastrointestinal tolerability from controlled release of SN-38 from novel polyoxazoline-modified dendrimers. Journal of Controlled Release 2017;247:73-85. [DOI: 10.1016/j.jconrel.2016.12.034] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 3.0] [Reference Citation Analysis]
69 Pan X, Liu Y, Li Z, Cui S, Gebru H, Xu J, Xu S, Liu J, Guo K. Amphiphilic Polyoxazoline- block -Polypeptoid Copolymers by Sequential One-Pot Ring-Opening Polymerizations. Macromol Chem Phys 2017;218:1600483. [DOI: 10.1002/macp.201600483] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 1.8] [Reference Citation Analysis]
70 Nam J, Jung Y, Jang W. Uracil-bearing poly(2-isopropyl-2-oxazoline): Hg( ii )-selective control of its thermoresponsiveness. Chem Commun 2017;53:11169-72. [DOI: 10.1039/c7cc06728c] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 1.8] [Reference Citation Analysis]
71 Hoogenboom R, Schlaad H. Thermoresponsive poly(2-oxazoline)s, polypeptoids, and polypeptides. Polym Chem 2017;8:24-40. [DOI: 10.1039/c6py01320a] [Cited by in Crossref: 192] [Cited by in F6Publishing: 193] [Article Influence: 32.0] [Reference Citation Analysis]
72 Tăbăcaru A, Furdui B, Ghinea IO, Cârâc G, Dinică RM. Recent advances in click chemistry reactions mediated by transition metal based systems. Inorganica Chimica Acta 2017;455:329-49. [DOI: 10.1016/j.ica.2016.07.029] [Cited by in Crossref: 42] [Cited by in F6Publishing: 35] [Article Influence: 7.0] [Reference Citation Analysis]
73 Su C, Huang C, Chen Y, Ger T. pH-responsive magnetic micelles gelatin-g-poly(NIPAAm-co-DMAAm-co-UA)-g-dextran/Fe 3 O 4 as a hydrophilic drug carrier. RSC Adv 2017;7:28207-12. [DOI: 10.1039/c7ra01633f] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 1.0] [Reference Citation Analysis]
74 Ying WB, Kim S, Lee MW, Go NY, Jung H, Ryu SG, Lee B, Lee KJ. Toward a detoxification fabric against nerve gas agents: guanidine-functionalized poly[2-(3-butenyl)-2-oxazoline]/Nylon-6,6 nanofibers. RSC Adv 2017;7:15246-54. [DOI: 10.1039/c7ra01278k] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 2.5] [Reference Citation Analysis]
75 Hartlieb M, Floyd T, Cook AB, Sanchez-cano C, Catrouillet S, Burns JA, Perrier S. Well-defined hyperstar copolymers based on a thiol–yne hyperbranched core and a poly(2-oxazoline) shell for biomedical applications. Polym Chem 2017;8:2041-54. [DOI: 10.1039/c7py00303j] [Cited by in Crossref: 28] [Cited by in F6Publishing: 28] [Article Influence: 4.7] [Reference Citation Analysis]
76 Glassner M, Palmieri L, Monnery BD, Verbrugghen T, Deleye S, Stroobants S, Staelens S, wyffels L, Hoogenboom R. The Label Matters: μPET Imaging of the Biodistribution of Low Molar Mass 89 Zr and 18 F-Labeled Poly(2-ethyl-2-oxazoline). Biomacromolecules 2017;18:96-102. [DOI: 10.1021/acs.biomac.6b01392] [Cited by in Crossref: 24] [Cited by in F6Publishing: 25] [Article Influence: 3.4] [Reference Citation Analysis]
77 Chen Y, Chen H, Feng M, Dong Y. Amphiphilic gradient copolymers: Synthesis, self-assembly, and applications. European Polymer Journal 2016;85:489-98. [DOI: 10.1016/j.eurpolymj.2016.11.009] [Cited by in Crossref: 26] [Cited by in F6Publishing: 26] [Article Influence: 3.7] [Reference Citation Analysis]
78 Park NH, Fevre M, Voo ZX, Ono RJ, Yang YY, Hedrick JL. Expanding the Cationic Polycarbonate Platform: Attachment of Sulfonium Moieties by Postpolymerization Ring Opening of Epoxides. ACS Macro Lett 2016;5:1247-52. [PMID: 35614734 DOI: 10.1021/acsmacrolett.6b00705] [Cited by in Crossref: 23] [Cited by in F6Publishing: 23] [Article Influence: 3.3] [Reference Citation Analysis]
79 Mees MA, Effenberg C, Appelhans D, Hoogenboom R. Sweet Polymers: Poly(2-ethyl-2-oxazoline) Glycopolymers by Reductive Amination. Biomacromolecules 2016;17:4027-36. [DOI: 10.1021/acs.biomac.6b01451] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 2.0] [Reference Citation Analysis]
80 Mees M, Haladjova E, Momekova D, Momekov G, Shestakova PS, Tsvetanov CB, Hoogenboom R, Rangelov S. Partially Hydrolyzed Poly( n -propyl-2-oxazoline): Synthesis, Aqueous Solution Properties, and Preparation of Gene Delivery Systems. Biomacromolecules 2016;17:3580-90. [DOI: 10.1021/acs.biomac.6b01088] [Cited by in Crossref: 32] [Cited by in F6Publishing: 32] [Article Influence: 4.6] [Reference Citation Analysis]
81 Sahn M, Yildirim T, Dirauf M, Weber C, Sungur P, Hoeppener S, Schubert US. LCST Behavior of Symmetrical PNiPAm- b -PEtOx- b -PNiPAm Triblock Copolymers. Macromolecules 2016;49:7257-67. [DOI: 10.1021/acs.macromol.6b01371] [Cited by in Crossref: 39] [Cited by in F6Publishing: 40] [Article Influence: 5.6] [Reference Citation Analysis]
82 Dargaville TR, Lava K, Verbraeken B, Hoogenboom R. Unexpected Switching of the Photogelation Chemistry When Cross-Linking Poly(2-oxazoline) Copolymers. Macromolecules 2016;49:4774-83. [DOI: 10.1021/acs.macromol.6b00167] [Cited by in Crossref: 31] [Cited by in F6Publishing: 31] [Article Influence: 4.4] [Reference Citation Analysis]
83 Kalaoglu-Altan OI, Verbraeken B, Lava K, Gevrek TN, Sanyal R, Dargaville T, De Clerck K, Hoogenboom R, Sanyal A. Multireactive Poly(2-oxazoline) Nanofibers through Electrospinning with Crosslinking on the Fly. ACS Macro Lett 2016;5:676-81. [PMID: 35614674 DOI: 10.1021/acsmacrolett.6b00188] [Cited by in Crossref: 34] [Cited by in F6Publishing: 34] [Article Influence: 4.9] [Reference Citation Analysis]
84 Kroneková Z, Mikulec M, Petrenčíková N, Paulovičová E, Paulovičová L, Jančinová V, Nosál' R, Reddy PS, Shimoga GD, Chorvát D, Kronek J. Ex Vivo and In Vitro Studies on the Cytotoxicity and Immunomodulative Properties of Poly(2-isopropenyl-2-oxazoline) as a New Type of Biomedical Polymer. Macromol Biosci 2016;16:1200-11. [DOI: 10.1002/mabi.201600016] [Cited by in Crossref: 21] [Cited by in F6Publishing: 22] [Article Influence: 3.0] [Reference Citation Analysis]
85 Driessen F, Martens S, Meyer BD, Du Prez FE, Espeel P. Double Modification of Polymer End Groups through Thiolactone Chemistry. Macromol Rapid Commun 2016;37:947-51. [DOI: 10.1002/marc.201600150] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 2.6] [Reference Citation Analysis]
86 Kim JH, Jung Y, Lee D, Jang WD. Thermoresponsive Polymer and Fluorescent Dye Hybrids for Tunable Multicolor Emission. Adv Mater 2016;28:3499-503. [PMID: 26990858 DOI: 10.1002/adma.201600043] [Cited by in Crossref: 53] [Cited by in F6Publishing: 53] [Article Influence: 7.6] [Reference Citation Analysis]
87 Rieger E, Manhart A, Wurm FR. Multihydroxy Polyamines by Living Anionic Polymerization of Aziridines. ACS Macro Lett 2016;5:195-8. [PMID: 35614699 DOI: 10.1021/acsmacrolett.5b00901] [Cited by in Crossref: 41] [Cited by in F6Publishing: 43] [Article Influence: 5.9] [Reference Citation Analysis]
88 Jerca VV, Lava K, Verbraeken B, Hoogenboom R. Poly(2-cycloalkyl-2-oxazoline)s: high melting temperature polymers solely based on Debye and Keesom van der Waals interactions. Polym Chem 2016;7:1309-22. [DOI: 10.1039/c5py01755f] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 2.4] [Reference Citation Analysis]
89 Vancoillie G, Brooks WLA, Mees MA, Sumerlin BS, Hoogenboom R. Synthesis of novel boronic acid-decorated poly(2-oxazoline)s showing triple-stimuli responsive behavior. Polym Chem 2016;7:6725-34. [DOI: 10.1039/c6py01437b] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 3.4] [Reference Citation Analysis]
90 Rother M, Nussbaumer MG, Renggli K, Bruns N. Protein cages and synthetic polymers: a fruitful symbiosis for drug delivery applications, bionanotechnology and materials science. Chem Soc Rev 2016;45:6213-49. [DOI: 10.1039/c6cs00177g] [Cited by in Crossref: 111] [Cited by in F6Publishing: 115] [Article Influence: 15.9] [Reference Citation Analysis]
91 Damodaran VB, Bhatnagar D, Murthy NS. Biomedical Polymers: Synthetic Strategies. Biomedical Polymers 2016. [DOI: 10.1007/978-3-319-32053-3_2] [Reference Citation Analysis]
92 de Jongh PAJM, Bennett MR, Sulley GS, Wilson P, Davis TP, Haddleton DM, Kempe K. Facile one-pot/one-step synthesis of heterotelechelic N-acylated poly(aminoester) macromonomers for carboxylic acid decorated comb polymers. Polym Chem 2016;7:6703-7. [DOI: 10.1039/c6py01553k] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 1.7] [Reference Citation Analysis]
93 Kim J, Yim D, Jang W. Thermo-responsive poly(2-isopropyl-2-oxazoline) and tetraphenylethene hybrids for stimuli-responsive photoluminescence control. Chem Commun 2016;52:4152-5. [DOI: 10.1039/c6cc00722h] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 3.1] [Reference Citation Analysis]
94 Fimberger M, Behrendt A, Jakopic G, Stelzer F, Kumbaraci V, Wiesbrock F. Modification Pathways for Copoly(2-oxazoline)s Enabling Their Application as Antireflective Coatings in Photolithography. Macromol Rapid Commun 2016;37:233-8. [PMID: 26619063 DOI: 10.1002/marc.201500589] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.9] [Reference Citation Analysis]
95 Billing M, Rudolph T, Täuscher E, Beckert R, Schacher F. Synthesis and Complexation of Well-Defined Labeled Poly(N,N-dimethylaminoethyl methacrylate)s (PDMAEMA). Polymers 2015;7:2478-93. [DOI: 10.3390/polym7121526] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 2.0] [Reference Citation Analysis]
96 Van Steenberge PHM, Verbraeken B, Reyniers M, Hoogenboom R, D’hooge DR. Model-Based Visualization and Understanding of Monomer Sequence Formation in Gradient Copoly(2-oxazoline)s On the basis of 2-Methyl-2-oxazoline and 2-Phenyl-2-oxazoline. Macromolecules 2015;48:7765-73. [DOI: 10.1021/acs.macromol.5b01642] [Cited by in Crossref: 28] [Cited by in F6Publishing: 29] [Article Influence: 3.5] [Reference Citation Analysis]
97 Le Fer G, Amiel C, Volet G. Copolymers based on azidopentyl-2-oxazoline: Synthesis, characterization and LCST behavior. European Polymer Journal 2015;71:523-33. [DOI: 10.1016/j.eurpolymj.2015.08.028] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 1.9] [Reference Citation Analysis]
98 Rueda JC, Asmad M, Ruiz V, Komber H, Zschoche S, Voit B. Synthesis and characterization of new bi-sensitive copoly(2-oxazolines). Designed Monomers and Polymers 2015;18:761-9. [DOI: 10.1080/15685551.2015.1078109] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
99 Vergaelen M, Verbraeken B, Monnery BD, Hoogenboom R. Sulfolane as Common Rate Accelerating Solvent for the Cationic Ring-Opening Polymerization of 2-Oxazolines. ACS Macro Lett 2015;4:825-8. [PMID: 35596503 DOI: 10.1021/acsmacrolett.5b00392] [Cited by in Crossref: 32] [Cited by in F6Publishing: 32] [Article Influence: 4.0] [Reference Citation Analysis]
100 Gaspar VM, Baril P, Costa EC, de Melo-Diogo D, Foucher F, Queiroz JA, Sousa F, Pichon C, Correia IJ. Bioreducible poly(2-ethyl-2-oxazoline)-PLA-PEI-SS triblock copolymer micelles for co-delivery of DNA minicircles and Doxorubicin. J Control Release 2015;213:175-91. [PMID: 26184050 DOI: 10.1016/j.jconrel.2015.07.011] [Cited by in Crossref: 67] [Cited by in F6Publishing: 68] [Article Influence: 8.4] [Reference Citation Analysis]
101 Kim J, Koo E, Ju S, Jang W. Multimodal Stimuli-Responsive Poly(2-isopropyl-2-oxazoline) with Dual Molecular Logic Gate Operations. Macromolecules 2015;48:4951-6. [DOI: 10.1021/acs.macromol.5b01046] [Cited by in Crossref: 26] [Cited by in F6Publishing: 27] [Article Influence: 3.3] [Reference Citation Analysis]
102 Bouten PJM, Hertsen D, Vergaelen M, Monnery BD, Catak S, van Hest JCM, Van Speybroeck V, Hoogenboom R. Synthesis of poly(2-oxazoline)s with side chain methyl ester functionalities: Detailed understanding of living copolymerization behavior of methyl ester containing monomers with 2-alkyl-2-oxazolines. J Polym Sci Part A: Polym Chem 2015;53:2649-61. [DOI: 10.1002/pola.27733] [Cited by in Crossref: 38] [Cited by in F6Publishing: 38] [Article Influence: 4.8] [Reference Citation Analysis]
103 Mees MA, Hoogenboom R. Functional Poly(2-oxazoline)s by Direct Amidation of Methyl Ester Side Chains. Macromolecules 2015;48:3531-8. [DOI: 10.1021/acs.macromol.5b00290] [Cited by in Crossref: 47] [Cited by in F6Publishing: 48] [Article Influence: 5.9] [Reference Citation Analysis]
104 Hayashi T, Takasu A. Design of Electrophoretic and Biocompatible Poly(2-oxazoline)s Initiated by Perfluoroalkanesulfoneimides and Electrophoretic Deposition with Bioactive Glass. Biomacromolecules 2015;16:1259-66. [DOI: 10.1021/acs.biomac.5b00043] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 2.8] [Reference Citation Analysis]
105 Sehlinger A, Verbraeken B, Meier MAR, Hoogenboom R. Versatile side chain modification via isocyanide-based multicomponent reactions: tuning the LCST of poly(2-oxazoline)s. Polym Chem 2015;6:3828-36. [DOI: 10.1039/c5py00392j] [Cited by in Crossref: 34] [Cited by in F6Publishing: 35] [Article Influence: 4.3] [Reference Citation Analysis]
106 Mansfield EDH, Sillence K, Hole P, Williams AC, Khutoryanskiy VV. POZylation: a new approach to enhance nanoparticle diffusion through mucosal barriers. Nanoscale 2015;7:13671-9. [DOI: 10.1039/c5nr03178h] [Cited by in Crossref: 55] [Cited by in F6Publishing: 55] [Article Influence: 6.9] [Reference Citation Analysis]
107 Glassner M, Maji S, de la Rosa VR, Vanparijs N, Ryskulova K, De Geest BG, Hoogenboom R. Solvent-free mechanochemical synthesis of a bicyclononyne tosylate: a fast route towards bioorthogonal clickable poly(2-oxazoline)s. Polym Chem 2015;6:8354-9. [DOI: 10.1039/c5py01280e] [Cited by in Crossref: 23] [Cited by in F6Publishing: 23] [Article Influence: 2.9] [Reference Citation Analysis]
108 Gieseler D, Jordan R. Poly(2-oxazoline) molecular brushes by grafting through of poly(2-oxazoline)methacrylates with aqueous ATRP. Polym Chem 2015;6:4678-89. [DOI: 10.1039/c5py00561b] [Cited by in Crossref: 28] [Cited by in F6Publishing: 29] [Article Influence: 3.5] [Reference Citation Analysis]