Mediating Reaction Orthogonality in Polymer and Materials Science.

Szczegóły
Abstrakt

Tytuł:: Mediating Reaction Orthogonality in Polymer and Materials Science.
Autorzy:: Corrigan N; Centre for Advanced Macromolecular Design and Australian Centre for Nanomedicine, School of Chemical Engineering, UNSW, Sydney, 2052, Australia.
Ciftci M; Centre for Advanced Macromolecular Design and Australian Centre for Nanomedicine, School of Chemical Engineering, UNSW, Sydney, 2052, Australia.; Department of Chemistry, Faculty of Engineering and Natural Science, Bursa Technical University, Bursa, 16310, Turkey.
Jung K; Centre for Advanced Macromolecular Design and Australian Centre for Nanomedicine, School of Chemical Engineering, UNSW, Sydney, 2052, Australia.
Boyer C; Centre for Advanced Macromolecular Design and Australian Centre for Nanomedicine, School of Chemical Engineering, UNSW, Sydney, 2052, Australia.
Źródło:: Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2021 Jan 25; Vol. 60 (4), pp. 1748-1781. Date of Electronic Publication: 2020 Sep 17.
Typ publikacji:: Journal Article; Review
Język:: English
Imprint Name(s):: Publication: <2004-> : Weinheim : Wiley-VCH
Original Publication: Weinheim/Bergstr. : New York, : Verlag Chemie ; Academic Press, c1962-
MeSH Terms:: Materials Science*
Polymers/*chemistry
Cycloaddition Reaction ; Photochemistry ; Solid-Phase Synthesis Techniques
References:: .
T. Xia, J. SantaLucia, M. E. Burkard, R. Kierzek, S. J. Schroeder, X. Jiao, C. Cox, D. H. Turner, Biochemistry 1998, 37, 14719-14735;.
S. Ainsworth, in Steady-State Enzyme Kinetics, Macmillan Education UK, London, 1977, pp. 1-28.
.
L. Zhang, E. Meggers, J. Am. Chem. Soc. 2005, 127, 74-75;.
Z. Chen, S. E. Boyken, M. Jia, F. Busch, D. Flores-Solis, M. J. Bick, P. Lu, Z. L. Van Aernum, A. Sahasrabuddhe, R. A. Langan, S. Bermeo, T. J. Brunette, V. K. Mulligan, L. P. Carter, F. DiMaio, N. G. Sgourakis, V. H. Wysocki, D. Baker, Nature 2019, 565, 106-111.
.
J. S. Lundeen, B. Sutherland, A. Patel, C. Stewart, C. Bamber, Nature 2011, 474, 188;.
G. Makey, Ö. Yavuz, D. K. Kesim, A. Turnalı, P. Elahi, S. Ilday, O. Tokel, F. Ö. Ilday, Nat. Photonics 2019, 13, 251-256.
G. Barany, R. B. Merrifield, J. Am. Chem. Soc. 1977, 99, 7363-7365.
.
C.-H. Wong, S. C. Zimmerman, Chem. Commun. 2013, 49, 1679-1695;.
C.-H. Wong, X.-S. Ye, Z. Zhang, J. Am. Chem. Soc. 1998, 120, 7137-7138;.
N. Corrigan, C. Boyer, ACS Macro Lett. 2019, 8, 812-818;.
D. Gräfe, A. Wickberg, M. M. Zieger, M. Wegener, E. Blasco, C. Barner-Kowollik, Nat. Commun. 2018, 9, 2788.
.
A. J. Teator, D. N. Lastovickova, C. W. Bielawski, Chem. Rev. 2016, 116, 1969-1992;.
F. A. Leibfarth, K. M. Mattson, B. P. Fors, H. A. Collins, C. J. Hawker, Angew. Chem. Int. Ed. 2013, 52, 199-210;.
Angew. Chem. 2013, 125, 210-222.
.
R. B. Merrifield, Angew. Chem. Int. Ed. Engl. 1985, 24, 799-810;.
Angew. Chem. 1985, 97, 801-812;.
R. N. Carmean, C. A. Figg, T. E. Becker, B. S. Sumerlin, Angew. Chem. Int. Ed. 2016, 55, 8624-8629;.
Angew. Chem. 2016, 128, 8766-8771.
.
M. A. Gauthier, M. I. Gibson, H. A. Klok, Angew. Chem. Int. Ed. 2009, 48, 48-58;.
Angew. Chem. 2009, 121, 50-60;.
S. Liu, K. T. Dicker, X. Jia, Chem. Commun. 2015, 51, 5218-5237.
.
R. K. Iha, K. L. Wooley, A. M. Nyström, D. J. Burke, M. J. Kade, C. J. Hawker, Chem. Rev. 2009, 109, 5620-5686;.
D. Manna, T. Udayabhaskararao, H. Zhao, R. Klajn, Angew. Chem. Int. Ed. 2015, 54, 12394-12397;.
Angew. Chem. 2015, 127, 12571-12574;.
M. A. Azagarsamy, K. S. Anseth, ACS Macro Lett. 2013, 2, 5-9;.
Y. Zou, L. Zhang, L. Yang, F. Zhu, M. M. Ding, F. Lin, Z. Wang, Y. W. Li, J. Controlled Release 2018, 273, 160-179.
.
M. J. Hansen, W. A. Velema, M. M. Lerch, W. Szymanski, B. L. Feringa, Chem. Soc. Rev. 2015, 44, 3358-3377;.
J. F. Reuther, S. D. Dahlhauser, E. V. Anslyn, Angew. Chem. Int. Ed. 2019, 58, 74-85;.
Angew. Chem. 2019, 131, 76-88;.
C. P. Ramil, Q. Lin, Chem. Commun. 2013, 49, 11007-11022.
C. G. Bochet, Synlett 2004, 2004, 2268-2274.
.
R. J. Levis, G. M. Menkir, H. Rabitz, Science 2001, 292, 709-713;.
A. Assion, T. Baumert, M. Bergt, T. Brixner, B. Kiefer, V. Seyfried, M. Strehle, G. Gerber, Science 1998, 282, 919-922.
G. Barany, F. Albericio, J. Am. Chem. Soc. 1985, 107, 4936-4942.
M. Schelhaas, H. Waldmann, Angew. Chem. Int. Ed. Engl. 1996, 35, 2056-2083;.
Angew. Chem. 1996, 108, 2192-2219.
P. Klán, T. Šolomek, C. G. Bochet, A. Blanc, R. Givens, M. Rubina, V. Popik, A. Kostikov, J. Wirz, Chem. Rev. 2013, 113, 119-191.
.
N. Zhang, W.-Y. Lo, A. Jose, Z. Cai, L. Li, L. Yu, Adv. Mater. 2017, 29, 1701248;.
M. M. Lerch, M. J. Hansen, W. A. Velema, W. Szymanski, B. L. Feringa, Nat. Commun. 2016, 7, 12054;.
J. R. Hemmer, S. O. Poelma, N. Treat, Z. A. Page, N. D. Dolinski, Y. J. Diaz, W. Tomlinson, K. D. Clark, J. P. Hooper, C. Hawker, J. Read de Alaniz, J. Am. Chem. Soc. 2016, 138, 13960-13966;.
S. Ishida, T. Fukaminato, D. Kitagawa, S. Kobatake, S. Kim, T. Ogata, S. Kurihara, Chem. Commun. 2017, 53, 8268-8271.
.
N. A. Afagh, A. K. Yudin, Angew. Chem. Int. Ed. 2010, 49, 262-310;.
Angew. Chem. 2010, 122, 270-320;.
A. Herner, Q. Lin, Top. Curr. Chem. 2015, 374, 1.
.
K. Morihiro, T. Kodama, S. Mori, S. Tsunoda, S. Obika, Org. Biomol. Chem. 2016, 14, 1555-1558;.
O. Eivgi, E. Levin, N. G. Lemcoff, Org. Lett. 2015, 17, 740-743.
.
A. Blanc, C. G. Bochet, J. Org. Chem. 2002, 67, 5567-5577;.
C. G. Bochet, Angew. Chem. Int. Ed. 2001, 40, 2071-2073;.
Angew. Chem. 2001, 113, 2140-2142;.
C. G. Bochet, Tetrahedron Lett. 2000, 41, 6341-6346.
A. del Campo, D. Boos, H. W. Spiess, U. Jonas, Angew. Chem. Int. Ed. 2005, 44, 4707-4712;.
Angew. Chem. 2005, 117, 4785-4791.
J.-L. Débieux, C. G. Bochet, Chem. Sci. 2012, 3, 405-406.
.
M. Shirai, M. Tsunooka, Prog. Polym. Sci. 1996, 21, 1-45;.
C. Sundararajan, D. E. Falvey, J. Am. Chem. Soc. 2005, 127, 8000-8001;.
J. B. Borak, H.-Y. Lee, S. R. Raghavan, D. E. Falvey, Chem. Commun. 2010, 46, 8983-8985;.
J. L. Norris, M. J. Hangauer, N. A. Porter, R. M. Caprioli, J. Mass Spectrom. 2005, 40, 1319-1326;.
M. C. Pirrung, L. Fallon, J. Zhu, Y. R. Lee, J. Am. Chem. Soc. 2001, 123, 3638-3643;.
P. Šebej, J. Wintner, P. Müller, T. Slanina, J. Al Anshori, L. A. P. Antony, P. Klán, J. Wirz, J. Org. Chem. 2013, 78, 1833-1843;.
P. Štacko, P. Šebej, A. T. Veetil, P. Klán, Org. Lett. 2012, 14, 4918-4921.
.
M. N. Stanton-Humphreys, R. D. T. Taylor, C. McDougall, M. L. Hart, C. T. A. Brown, N. J. Emptage, S. J. Conway, Chem. Commun. 2012, 48, 657-659;.
A. Gautier, C. Gauron, M. Volovitch, D. Bensimon, L. Jullien, S. Vriz, Nat. Chem. Biol. 2014, 10, 533;.
L. Fournier, C. Gauron, L. Xu, I. Aujard, T. Le Saux, N. Gagey-Eilstein, S. Maurin, S. Dubruille, J.-B. Baudin, D. Bensimon, M. Volovitch, S. Vriz, L. Jullien, ACS Chem. Biol. 2013, 8, 1528-1536.
M. A. Azagarsamy, K. S. Anseth, Angew. Chem. Int. Ed. 2013, 52, 13803-13807;.
Angew. Chem. 2013, 125, 14048-14052.
.
B. N. Goguen, A. Aemissegger, B. Imperiali, J. Am. Chem. Soc. 2011, 133, 11038-11041;.
S. Kantevari, M. Matsuzaki, Y. Kanemoto, H. Kasai, G. C. R. Ellis-Davies, Nat. Methods 2010, 7, 123;.
P. Stegmaier, J. M. Alonso, A. d. Campo, Langmuir 2008, 24, 11872-11879;.
J. P. Olson, M. R. Banghart, B. L. Sabatini, G. C. R. Ellis-Davies, J. Am. Chem. Soc. 2013, 135, 15948-15954;.
C. Menge, A. Heckel, Org. Lett. 2011, 13, 4620-4623;.
N. Kotzur, B. Briand, M. Beyermann, V. Hagen, J. Am. Chem. Soc. 2009, 131, 16927-16931;.
M. A. Priestman, L. Sun, D. S. Lawrence, ACS Chem. Biol. 2011, 6, 377-384;.
S. Yamazoe, Q. Liu, L. E. McQuade, A. Deiters, J. K. Chen, Angew. Chem. Int. Ed. 2014, 53, 10114-10118;.
Angew. Chem. 2014, 126, 10278-10282;.
M. Wu, X. Lin, X. Tan, J. Li, Z. Wei, D. Zhang, Y. Zheng, A.-x. Zheng, B. Zhao, Y. Zeng, X. Liu, J. Liu, ACS Appl. Mater. Interfaces 2018, 10, 19416-19427.
V. San Miguel, C. G. Bochet, A. del Campo, J. Am. Chem. Soc. 2011, 133, 5380-5388.
X. Hu, Z. Qureishi, S. W. Thomas, Chem. Mater. 2017, 29, 2951-2960.
.
H. Inui, S. Murata, J. Am. Chem. Soc. 2005, 127, 2628-2636;.
J. Li, H. Kong, L. Huang, B. Cheng, K. Qin, M. Zheng, Z. Yan, Y. Zhang, J. Am. Chem. Soc. 2018, 140, 14542-14546;.
H. A. Houck, F. E. Du Prez, C. Barner-Kowollik, Nat. Commun. 2017, 8, 1869;.
B. J. Arnold, S. M. Mellows, P. G. Sammes, T. W. Wallace, J. Chem. Soc. Perkin Trans. 1 1974, 401-409.
P. Lederhose, D. Abt, A. Welle, R. Müller, C. Barner-Kowollik, J. P. Blinco, Chem. Eur. J. 2018, 24, 576-580.
.
J. P. Menzel, F. Feist, B. Tuten, T. Weil, J. P. Blinco, C. Barner-Kowollik, Angew. Chem. Int. Ed. 2019, 58, 7470-7474;.
Angew. Chem. 2019, 131, 7548-7552;.
J. P. Menzel, B. B. Noble, A. Lauer, M. L. Coote, J. P. Blinco, C. Barner-Kowollik, J. Am. Chem. Soc. 2017, 139, 15812-15820;.
F. Feist, J. P. Menzel, T. Weil, J. P. Blinco, C. Barner-Kowollik, J. Am. Chem. Soc. 2018, 140, 11848-11854.
.
R. Remy, C. G. Bochet, Chem. Rev. 2016, 116, 9816-9849;.
M. A. Tasdelen, Y. Yagci, Angew. Chem. Int. Ed. 2013, 52, 5930-5938;.
Angew. Chem. 2013, 125, 6044-6053;.
L. M. T. Frija, A. Ismael, M. L. S. Cristiano, Molecules 2010, 15, 3757-3774;.
M. Meldal, C. W. Tornøe, Chem. Rev. 2008, 108, 2952-3015;.
F. Mueller, J. Mattay, Chem. Rev. 1993, 93, 99-117.
.
C. E. Hoyle, C. N. Bowman, Angew. Chem. Int. Ed. 2010, 49, 1540-1573;.
Angew. Chem. 2010, 122, 1584-1617;.
C. E. Hoyle, T. Y. Lee, T. Roper, J. Polym. Sci. Part A 2004, 42, 5301-5338;.
M. J. Kade, D. J. Burke, C. J. Hawker, J. Polym. Sci. Part A 2010, 48, 743-750;.
B. D. Mather, K. Viswanathan, K. M. Miller, T. E. Long, Prog. Polym. Sci. 2006, 31, 487-531.
.
P. Antoni, M. J. Robb, L. Campos, M. Montanez, A. Hult, E. Malmström, M. Malkoch, C. J. Hawker, Macromolecules 2010, 43, 6625-6631;.
K. L. Killops, L. M. Campos, C. J. Hawker, J. Am. Chem. Soc. 2008, 130, 5062-5064;.
B. D. Fairbanks, M. P. Schwartz, A. E. Halevi, C. R. Nuttelman, C. N. Bowman, K. S. Anseth, Adv. Mater. 2009, 21, 5005-5010;.
N. Gupta, B. F. Lin, L. M. Campos, M. D. Dimitriou, S. T. Hikita, N. D. Treat, M. V. Tirrell, D. O. Clegg, E. J. Kramer, C. J. Hawker, Nat. Chem. 2010, 2, 138;.
P. J. LeValley, E. M. Ovadia, C. A. Bresette, L. A. Sawicki, E. Maverakis, S. Bai, A. M. Kloxin, Chem. Commun. 2018, 54, 6923-6926.
.
N. B. Cramer, S. K. Reddy, A. K. O'Brien, C. N. Bowman, Macromolecules 2003, 36, 7964-7969;.
S. K. Reddy, N. B. Cramer, C. N. Bowman, Macromolecules 2006, 39, 3673-3680;.
T. M. Roper, C. A. Guymon, E. S. Jönsson, C. E. Hoyle, J. Polym. Sci. Part A 2004, 42, 6283-6298.
.
B. D. Fairbanks, T. F. Scott, C. J. Kloxin, K. S. Anseth, C. N. Bowman, Macromolecules 2009, 42, 211-217;.
R. Hoogenboom, Angew. Chem. Int. Ed. 2010, 49, 3415-3417;.
Angew. Chem. 2010, 122, 3489-3491;.
A. B. Lowe, C. E. Hoyle, C. N. Bowman, J. Mater. Chem. 2010, 20, 4745-4750.
J. W. Chan, C. E. Hoyle, A. B. Lowe, J. Am. Chem. Soc. 2009, 131, 5751-5753.
.
S. Poplata, A. Tröster, Y.-Q. Zou, T. Bach, Chem. Rev. 2016, 116, 9748-9815;.
V. Ramamurthy, J. Sivaguru, Chem. Rev. 2016, 116, 9914-9993;.
N. Corrigan, S. Shanmugam, J. Xu, C. Boyer, Chem. Soc. Rev. 2016, 45, 6165-6212;.
T. Junkers, Eur. Polym. J. 2015, 62, 273-280.
G. Kaur, P. Johnston, K. Saito, Polym. Chem. 2014, 5, 2171-2186.
.
S. R. Trenor, A. R. Shultz, B. J. Love, T. E. Long, Chem. Rev. 2004, 104, 3059-3078;.
J.-F. Xu, Y.-Z. Chen, L.-Z. Wu, C.-H. Tung, Q.-Z. Yang, Org. Lett. 2013, 15, 6148-6151;.
J. Van Damme, F. Du Prez, Prog. Polym. Sci. 2018, 82, 92-119;.
H. Bouas-Laurent, A. Castellan, J.-P. Desvergne, R. Lapouyade, Chem. Soc. Rev. 2000, 29, 43-55.
Y. Yagci, S. Jockusch, N. J. Turro, Macromolecules 2010, 43, 6245-6260.
.
M. Ciftci, S. Kork, G. Xu, M. R. Buchmeiser, Y. Yagci, Macromolecules 2015, 48, 1658-1663;.
C. E. Hoyle, A. B. Lowe, C. N. Bowman, Chem. Soc. Rev. 2010, 39, 1355-1387;.
B. J. Adzima, Y. Tao, C. J. Kloxin, C. A. DeForest, K. S. Anseth, C. N. Bowman, Nat. Chem. 2011, 3, 256;.
M. Ciftci, M. A. Tasdelen, Y. Yagci, Polym. Int. 2016, 65, 1001-1014.
H. F. Gruber, Prog. Polym. Sci. 1992, 17, 953-1044.
C. N. LaFratta, J. T. Fourkas, T. Baldacchini, R. A. Farrer, Angew. Chem. Int. Ed. 2007, 46, 6238-6258;.
Angew. Chem. 2007, 119, 6352-6374.
J. V. Crivello, J. H. W. Lam, Macromolecules 1977, 10, 1307-1315.
.
Y. Matano, T. Shinokura, O. Yoshikawa, H. Imahori, Org. Lett. 2008, 10, 2167-2170;.
M. Jin, X. Wu, J. Xie, J. P. Malval, D. Wan, RSC Adv. 2015, 5, 55340-55347.
L. Atmaca, I. Kayihan, Y. Yagci, Polymer 2000, 41, 6035-6041.
H.-Q. Guo, A. Kajiwara, Y. Morishima, M. Kamachi, Polym. J. 1996, 28, 960-964.
J. V. Crivello, J. Polym. Sci. Part A 1999, 37, 4241-4254.
.
J. V. Crivello, J. Polym. Sci. Part A 2009, 47, 866-875;.
M. Ciftci, Y. Yoshikawa, Y. Yagci, Angew. Chem. Int. Ed. 2017, 56, 519-523;.
Angew. Chem. 2017, 129, 534-538.
D. Dossow, Z. Qin Qin, G. Hizal, Y. Yagci, W. Schnabel, Polymer 1996, 37, 2821-2826.
G. Hizal, Y. Yagci, W. Schnabel, Polymer 1994, 35, 2428-2431.
.
S. Dadashi-Silab, S. Doran, Y. Yagci, Chem. Rev. 2016, 116, 10212-10275;.
M. Sangermano, I. Roppolo, A. Chiappone, Polymers 2018, 10, 136.
T. P. Yoon, M. A. Ischay, J. Du, Nat. Chem. 2010, 2, 527.
.
M. Ciftci, M. A. Tasdelen, Y. Yagci, Polym. Chem. 2014, 5, 600-606;.
N. J. Treat, H. Sprafke, J. W. Kramer, P. G. Clark, B. E. Barton, J. Read de Alaniz, B. P. Fors, C. J. Hawker, J. Am. Chem. Soc. 2014, 136, 16096-16101;.
C. K. Prier, D. A. Rankic, D. W. C. MacMillan, Chem. Rev. 2013, 113, 5322-5363;.
J. M. R. Narayanam, C. R. J. Stephenson, Chem. Soc. Rev. 2011, 40, 102-113.
.
Y. Xi, H. Yi, A. Lei, Org. Biomol. Chem. 2013, 11, 2387-2403;.
N. Zivic, M. Bouzrati-Zerelli, A. Kermagoret, F. Dumur, J.-P. Fouassier, D. Gigmes, J. Lalevée, ChemCatChem 2016, 8, 1617-1631.
.
A. Eibel, D. E. Fast, J. Sattelkow, M. Zalibera, J. Wang, A. Huber, G. Müller, D. Neshchadin, K. Dietliker, H. Plank, H. Grützmacher, G. Gescheidt, Angew. Chem. Int. Ed. 2017, 56, 14306-14309;.
Angew. Chem. 2017, 129, 14496-14499;.
F. Zeng, S. C. Zimmerman, J. Am. Chem. Soc. 1996, 118, 5326-5327;.
X.-X. Deng, F.-S. Du, Z.-C. Li, ACS Macro Lett. 2014, 3, 667-670;.
N. Kottari, Y. M. Chabre, T. C. Shiao, R. Rej, R. Roy, Chem. Commun. 2014, 50, 1983-1985.
N. Zydziak, F. Feist, B. Huber, J. O. Mueller, C. Barner-Kowollik, Chem. Commun. 2015, 51, 1799-1802.
N. Zydziak, W. Konrad, F. Feist, S. Afonin, S. Weidner, C. Barner-Kowollik, Nat. Commun. 2016, 7, 13672.
M. Van De Walle, K. De Bruycker, T. Junkers, J. P. Blinco, C. Barner-Kowollik, ChemPhotoChem 2019, 3, 225-228.
J. Xu, C. Fu, S. Shanmugam, C. J. Hawker, G. Moad, C. Boyer, Angew. Chem. Int. Ed. 2017, 56, 8376-8383;.
Angew. Chem. 2017, 129, 8496-8503.
.
J. C. Barnes, D. J. C. Ehrlich, A. X. Gao, F. A. Leibfarth, Y. Jiang, E. Zhou, T. F. Jamison, J. A. Johnson, Nat. Chem. 2015, 7, 810;.
F. Amir, Z. Jia, M. J. Monteiro, J. Am. Chem. Soc. 2016, 138, 16600-16603;.
S. Martens, J. Van den Begin, A. Madder, F. E. Du Prez, P. Espeel, J. Am. Chem. Soc. 2016, 138, 14182-14185;.
C. Fu, Z. Huang, C. J. Hawker, G. Moad, J. Xu, C. Boyer, Polym. Chem. 2017, 8, 4637-4643.
M. Porel, C. A. Alabi, J. Am. Chem. Soc. 2014, 136, 13162-13165.
W. H. Binder, R. Sachsenhofer, Macromol. Rapid Commun. 2008, 29, 952-981.
K. Hiltebrandt, T. Pauloehrl, J. P. Blinco, K. Linkert, H. G. Borner, C. Barner-Kowollik, Angew. Chem. Int. Ed. 2015, 54, 2838-2843;.
Angew. Chem. 2015, 127, 2880-2885.
K. Hiltebrandt, M. Kaupp, E. Molle, J. P. Menzel, J. P. Blinco, C. Barner-Kowollik, Chem. Commun. 2016, 52, 9426-9429.
E. H. Discekici, A. H. St Amant, S. N. Nguyen, I.-H. Lee, C. J. Hawker, J. Read de Alaniz, J. Am. Chem. Soc. 2018, 140, 5009-5013.
M. Kaupp, K. Hiltebrandt, V. Trouillet, P. Mueller, A. S. Quick, M. Wegener, C. Barner-Kowollik, Chem. Commun. 2016, 52, 1975-1978.
R. R. Batchelor, E. Blasco, K. N. R. Wuest, H. Lu, M. Wegener, C. Barner-Kowollik, M. H. Stenzel, Chem. Commun. 2018, 54, 2436-2439.
M. M. Zieger, P. Mueller, A. S. Quick, M. Wegener, C. Barner-Kowollik, Angew. Chem. Int. Ed. 2017, 56, 5625-5629;.
Angew. Chem. 2017, 129, 5717-5721.
.
H. Frisch, F. R. Bloesser, C. Barner-Kowollik, Angew. Chem. Int. Ed. 2019, 58, 3604-3609;.
Angew. Chem. 2019, 131, 3642-3648;.
D. E. Marschner, H. Frisch, J. T. Offenloch, B. T. Tuten, C. R. Becer, A. Walther, A. S. Goldmann, P. Tzvetkova, C. Barner-Kowollik, Macromolecules 2018, 51, 3802-3807.
.
T. K. Claus, S. Telitel, A. Welle, M. Bastmeyer, A. P. Vogt, G. Delaittre, C. Barner-Kowollik, Chem. Commun. 2017, 53, 1599-1602;.
H. Frisch, D. Kodura, F. R. Bloesser, L. Michalek, C. Barner-Kowollik, Macromol. Rapid Commun. 2019, 40, 1900414.
B. P. Fors, C. J. Hawker, Angew. Chem. Int. Ed. 2012, 51, 8850-8853;.
Angew. Chem. 2012, 124, 8980-8983.
M. Kang, B. Moon, Macromolecules 2009, 42, 455-458.
N. De Alwis Watuthanthrige, P. N. Kurek, D. Konkolewicz, Polym. Chem. 2018, 9, 1557-1561.
Q. Yan, D. Han, Y. Zhao, Polym. Chem. 2013, 4, 5026-5037.
A. Bagheri, J. Yeow, H. Arandiyan, J. Xu, C. Boyer, M. Lim, Macromol. Rapid Commun. 2016, 37, 905-910.
S. Xu, J. Yeow, C. Boyer, ACS Macro Lett. 2018, 7, 1376-1382.
Q. A. Jin, G. Y. Liu, J. A. Li, Eur. Polym. J. 2010, 46, 2120-2128.
M. Chen, S. Deng, Y. Gu, J. Lin, M. J. MacLeod, J. A. Johnson, J. Am. Chem. Soc. 2017, 139, 2257-2266.
S. Shanmugam, J. T. Xu, C. Boyer, Polym. Chem. 2016, 7, 6437-6449.
.
C. Wu, H. Chen, N. Corrigan, K. Jung, X. Kan, Z. Li, W. Liu, J. Xu, C. Boyer, J. Am. Chem. Soc. 2019, 141, 8207-8220.
A. Keyes, H. E. Basbug Alhan, U. Ha, Y.-S. Liu, S. K. Smith, T. S. Teets, D. B. Beezer, E. Harth, Macromolecules 2018, 51, 7224-7232.
R. L. Sutar, E. Levin, D. Butilkov, I. Goldberg, O. Reany, N. G. Lemcoff, Angew. Chem. Int. Ed. 2016, 55, 764-767;.
Angew. Chem. 2016, 128, 774-777.
.
S. Villarroya, J. Zhou, K. J. Thurecht, S. M. Howdle, Macromolecules 2006, 39, 9080-9086;.
F. Li, W. Yang, M. Li, L. Lei, Polym. Chem. 2019, 10, 3996-4005.
C. Fu, J. Xu, M. Kokotovic, C. Boyer, ACS Macro Lett. 2016, 5, 444-449.
C. K. Fu, J. T. Xu, C. Boyer, Chem. Commun. 2016, 52, 7126-7129.
B. M. Peterson, V. Kottisch, M. J. Supej, B. P. Fors, ACS Cent. Sci. 2018, 4, 1228-1234.
V. Kottisch, Q. Michaudel, B. P. Fors, J. Am. Chem. Soc. 2017, 139, 10665-10668.
A. Ohtsuki, L. Lei, M. Tanishima, A. Goto, H. Kaji, J. Am. Chem. Soc. 2015, 137, 5610-5617.
Z. Zhang, T.-Y. Zeng, L. Xia, C.-Y. Hong, D.-C. Wu, Y.-Z. You, Nat. Commun. 2018, 9, 2577.
J. T. Xu, S. Shanmugam, C. K. Fu, K. F. Aguey-Zinsou, C. Boyer, J. Am. Chem. Soc. 2016, 138, 3094-3106.
S. Shanmugam, J. Cuthbert, T. Kowalewski, C. Boyer, K. Matyjaszewski, Macromolecules 2018, 51, 7776-7784.
S. Shanmugam, J. Cuthbert, J. Flum, M. Fantin, C. Boyer, T. Kowalewski, K. Matyjaszewski, Polym. Chem. 2019, 10, 2477-2483.
J. M. Zhuang, M. R. Gordon, J. Ventura, L. Y. Li, S. Thayumanavan, Chem. Soc. Rev. 2013, 42, 7421-7435.
T. Krappitz, F. Feist, I. Lamparth, N. Moszner, H. John, J. P. Blinco, T. R. Dargaville, C. Barner-Kowollik, Mater. Horiz. 2019, 6, 81-89.
V. X. Truong, F. Li, F. Ercole, J. S. Forsythe, ACS Macro Lett. 2018, 7, 464-469.
V. X. Truong, F. Li, J. S. Forsythe, ACS Macro Lett. 2017, 6, 657-662.
A. M. Schenzel, N. Moszner, C. Barner-Kowollik, ACS Macro Lett. 2017, 6, 16-20.
C. P. Kabb, C. S. O'Bryan, C. C. Deng, T. E. Angelini, B. S. Sumerlin, ACS Appl. Mater. Interfaces 2018, 10, 16793-16801.
L. García-Fernández, C. Herbivo, V. S. M. Arranz, D. Warther, L. Donato, A. Specht, A. del Campo, Adv. Mater. 2014, 26, 5012-5017.
C. A. DeForest, B. D. Polizzotti, K. S. Anseth, Nat. Mater. 2009, 8, 659.
E. R. Draper, E. G. B. Eden, T. O. McDonald, D. J. Adams, Nat. Chem. 2015, 7, 848.
C. A. DeForest, E. A. Sims, K. S. Anseth, Chem. Mater. 2010, 22, 4783-4790.
D. Klinger, K. Landfester, Macromolecules 2011, 44, 9758-9772.
D. Klinger, K. Landfester, J. Polym. Sci. Part A 2012, 50, 1062-1075.
T. F. Scott, B. A. Kowalski, A. C. Sullivan, C. N. Bowman, R. R. McLeod, Science 2009, 324, 913-917.
Z. Gan, Y. Cao, R. A. Evans, M. Gu, Nat. Commun. 2013, 4, 2061.
X. Xiong, L. Xue, J. Cui, ACS Macro Lett. 2018, 7, 239-243.
.
X. Zhang, W. Xi, S. Huang, K. Long, C. N. Bowman, Macromolecules 2017, 50, 5652-5660;.
P. K. Shah, J. W. Stansbury, C. N. Bowman, Polym. Chem. 2017, 8, 4339-4351;.
W. Xi, H. Peng, A. Aguirre-Soto, C. J. Kloxin, J. W. Stansbury, C. N. Bowman, Macromolecules 2014, 47, 6159-6165;.
K. N. Zhu, G. H. Liu, G. Y. Zhang, J. M. Hu, S. Y. Liu, Macromolecules 2018, 51, 8530-8538.
.
X. Zhang, L. Cox, Z. Wen, W. Xi, Y. Ding, C. N. Bowman, Polymer 2018, 156, 162-168;.
O. Konuray, X. Fernandez-Francos, X. Ramis, A. Serra, Polymers 2018, 10, 178.
H. Y. Peng, D. P. Nair, B. A. Kowalski, W. X. Xi, T. Gong, C. Wang, M. Cole, N. B. Cramer, X. L. Xie, R. R. McLeod, C. N. Bowman, Macromolecules 2014, 47, 2306-2315.
H. Y. Peng, C. Wang, W. X. Xi, B. A. Kowalski, T. Gong, X. L. Xie, W. T. Wang, D. P. Nair, R. R. McLeod, C. N. Bowman, Chem. Mater. 2014, 26, 6819-6826.
S. Bialas, L. Michalek, D. E. Marschner, T. Krappitz, M. Wegener, J. Blinco, E. Blasco, H. Frisch, C. Barner-Kowollik, Adv. Mater. 2019, 31, 1807288.
.
W. Wang, X. Sun, W. Wu, H. Peng, Y. Yu, Angew. Chem. Int. Ed. 2012, 51, 4644-4647;.
Angew. Chem. 2012, 124, 4722-4725;.
R. R. Kohlmeyer, J. Chen, Angew. Chem. Int. Ed. 2013, 52, 9234-9237;.
Angew. Chem. 2013, 125, 9404-9407.
L. Yu, Q. Wang, J. Sun, C. Li, C. Zou, Z. He, Z. Wang, L. Zhou, L. Zhang, H. Yang, J. Mater. Chem. A 2015, 3, 13953-13961.
.
P. Chakma, D. Konkolewicz, Angew. Chem. Int. Ed. 2019, 58, 9682-9695;.
Angew. Chem. 2019, 131, 9784-9797;.
C. J. Kloxin, C. N. Bowman, Chem. Soc. Rev. 2013, 42, 7161-7173.
.
X. Chen, M. A. Dam, K. Ono, A. Mal, H. Shen, S. R. Nutt, K. Sheran, F. Wudl, Science 2002, 295, 1698;.
D. Montarnal, M. Capelot, F. Tournilhac, L. Leibler, Science 2011, 334, 965;.
C. N. Bowman, C. J. Kloxin, Angew. Chem. Int. Ed. 2012, 51, 4272-4274;.
Angew. Chem. 2012, 124, 4346-4348;.
Z. P. Zhang, M. Z. Rong, M. Q. Zhang, Prog. Polym. Sci. 2018, 80, 39-93.
H. Y. Jiang, S. Kelch, A. Lendlein, Adv. Mater. 2006, 18, 1471-1475.
T. F. Scott, A. D. Schneider, W. D. Cook, C. N. Bowman, Science 2005, 308, 1615.
.
S. Wu, H.-J. Butt, Adv. Mater. 2016, 28, 1208-1226;.
J. Liu, W. Bu, L. Pan, J. Shi, Angew. Chem. Int. Ed. 2013, 52, 4375-4379;.
Angew. Chem. 2013, 125, 4471-4475;.
Z. Chen, S. He, H.-J. Butt, S. Wu, Adv. Mater. 2015, 27, 2203-2206.
Y. Yang, Z. Pei, X. Zhang, L. Tao, Y. Wei, Y. Ji, Chem. Sci. 2014, 5, 3486-3492.
Y. Yang, Z. Pei, Z. Li, Y. Wei, Y. Ji, J. Am. Chem. Soc. 2016, 138, 2118-2121.
Y. Amamoto, J. Kamada, H. Otsuka, A. Takahara, K. Matyjaszewski, Angew. Chem. Int. Ed. 2011, 50, 1660-1663;.
Angew. Chem. 2011, 123, 1698-1701.
Y. Amamoto, H. Otsuka, A. Takahara, K. Matyjaszewski, ACS Macro Lett. 2012, 1, 478-481.
Y. Amamoto, H. Otsuka, A. Takahara, K. Matyjaszewski, Adv. Mater. 2012, 24, 3975-3980.
.
S. Telitel, Y. Amamoto, J. Poly, F. Morlet-Savary, O. Soppera, J. Lalevée, K. Matyjaszewski, Polym. Chem. 2014, 5, 921-930;.
M. Herder, J.-M. Lehn, J. Am. Chem. Soc. 2018, 140, 7647-7657;.
H. Otsuka, Polym. J. 2013, 45, 879.
.
B. T. Michal, C. A. Jaye, E. J. Spencer, S. J. Rowan, ACS Macro Lett. 2013, 2, 694-699;.
H. Otsuka, S. Nagano, Y. Kobashi, T. Maeda, A. Takahara, Chem. Commun. 2010, 46, 1150-1152.
B. Ghosh, M. W. Urban, Science 2009, 323, 1458.
S. Ji, W. Cao, Y. Yu, H. Xu, Adv. Mater. 2015, 27, 7740-7745.
.
J. Ling, M. Z. Rong, M. Q. Zhang, Polymer 2012, 53, 2691-2698;.
S. Banerjee, R. Tripathy, D. Cozzens, T. Nagy, S. Keki, M. Zsuga, R. Faust, ACS Appl. Mater. Interfaces 2015, 7, 2064-2072.
P. Froimowicz, H. Frey, K. Landfester, Macromol. Rapid Commun. 2011, 32, 468-473.
.
N. Kuhl, S. Bode, M. D. Hager, U. S. Schubert, in Self-healing Materials (Eds.: M. D. Hager, S. van der Zwaag, U. S. Schubert), Springer International Publishing, Cham, 2016, pp. 1-58;.
Y. Yang, X. Ding, M. W. Urban, Prog. Polym. Sci. 2015, 49-50, 34-59;.
C. J. Kloxin, T. F. Scott, B. J. Adzima, C. N. Bowman, Macromolecules 2010, 43, 2643-2653;.
J. V. Accardo, J. A. Kalow, Chem. Sci. 2018, 9, 5987-5993;.
D. Habault, H. Zhang, Y. Zhao, Chem. Soc. Rev. 2013, 42, 7244-7256;.
A. J. R. Amaral, G. Pasparakis, Polym. Chem. 2017, 8, 6464-6484;.
C.-M. Chung, Y.-S. Roh, S.-Y. Cho, J.-G. Kim, Chem. Mater. 2004, 16, 3982-3984.
M. B. Gordon, J. M. French, N. J. Wagner, C. J. Kloxin, Adv. Mater. 2015, 27, 8007-8010.
L. A. Connal, R. Vestberg, C. J. Hawker, G. G. Qiao, Adv. Funct. Mater. 2008, 18, 3315-3322.
.
G. Widawski, M. Rawiso, B. François, Nature 1994, 369, 387-389;.
A. Zhang, H. Bai, L. Li, Chem. Rev. 2015, 115, 9801-9868.
T. F. Scott, R. B. Draughon, C. N. Bowman, Adv. Mater. 2006, 18, 2128-2132.
C. J. Kloxin, T. F. Scott, H. Y. Park, C. N. Bowman, Adv. Mater. 2011, 23, 1977-1981.
M. K. McBride, M. Hendrikx, D. Liu, B. T. Worrell, D. J. Broer, C. N. Bowman, Adv. Mater. 2017, 29, 1606509.
M. K. McBride, A. M. Martinez, L. Cox, M. Alim, K. Childress, M. Beiswinger, M. Podgorski, B. T. Worrell, J. Killgore, C. N. Bowman, Sci. Adv. 2018, 4, eaat4634.
B. T. Worrell, M. K. McBride, G. B. Lyon, L. M. Cox, C. Wang, S. Mavila, C.-H. Lim, H. M. Coley, C. B. Musgrave, Y. Ding, C. N. Bowman, Nat. Commun. 2018, 9, 2804.
N. D. Dolinski, Z. A. Page, E. B. Callaway, F. Eisenreich, R. V. Garcia, R. Chavez, D. P. Bothman, S. Hecht, F. W. Zok, C. J. Hawker, Adv. Mater. 2018, 30, 1800364.
J. J. Schwartz, A. J. Boydston, Nat. Commun. 2019, 10, 791.
.
A. J. Boydston, B. Cao, A. Nelson, R. J. Ono, A. Saha, J. J. Schwartz, C. J. Thrasher, J. Mater. Chem. A 2018, 6, 20621-20645;.
X. Kuang, D. J. Roach, J. Wu, C. M. Hamel, Z. Ding, T. Wang, M. L. Dunn, H. J. Qi, Adv. Funct. Mater. 2019, 29, 1805290;.
L. Huang, R. Jiang, J. Wu, J. Song, H. Bai, B. Li, Q. Zhao, T. Xie, Adv. Mater. 2017, 29, 1605390;.
Z. Zhang, N. Corrigan, A. Bagheri, J. Jin, C. A. J. M. Boyer, Angew. Chem. Int. Ed. 2019, 58, 17954-17963;.
Angew. Chem. 2019, 131, 18122-18131.
Z. Zhao, J. Wu, X. Mu, H. Chen, H. J. Qi, D. Fang, Macromol. Rapid Commun. 2017, 38, 1600625.
Q. Ge, A. H. Sakhaei, H. Lee, C. K. Dunn, N. X. Fang, M. L. Dunn, Sci. Rep. 2016, 6, 31110.
B. Zhang, K. Kowsari, A. Serjouei, M. L. Dunn, Q. Ge, Nat. Commun. 2018, 9, 1831.
R. Noyori, Nat. Chem. 2009, 1, 5.
.
A. Coskun, M. Banaszak, R. D. Astumian, J. F. Stoddart, B. A. Grzybowski, Chem. Soc. Rev. 2012, 41, 19-30;.
G. De Bo, M. A. Y. Gall, S. Kuschel, J. De Winter, P. Gerbaux, D. A. Leigh, Nat. Nanotechnol. 2018, 13, 381-385;.
S. Kassem, A. T. L. Lee, D. A. Leigh, V. Marcos, L. I. Palmer, S. Pisano, Nature 2017, 549, 374;.
B. Lewandowski, G. De Bo, J. W. Ward, M. Papmeyer, S. Kuschel, M. J. Aldegunde, P. M. E. Gramlich, D. Heckmann, S. M. Goldup, D. M. D′Souza, A. E. Fernandes, D. A. Leigh, Science 2013, 339, 189-193;.
W. 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, A. J. Turberfield, Nat. Chem. 2016, 8, 542;.
H. Sell, A. Gehl, D. Plaul, F. D. Sönnichsen, C. Schütt, F. Köhler, K. Steinborn, R. Herges, Commun. Chem. 2019, 2, 62.
K. H. Bleicher, H.-J. Böhm, K. Müller, A. I. Alanine, Nat. Rev. Drug Discovery 2003, 2, 369-378.
H. Frisch, D. E. Marschner, A. S. Goldmann, C. Barner-Kowollik, Angew. Chem. Int. Ed. 2018, 57, 2036-2045;.
Angew. Chem. 2018, 130, 2054-2064.
.
J. M. Caruthers, J. A. Lauterbach, K. T. Thomson, V. Venkatasubramanian, C. M. Snively, A. Bhan, S. Katare, G. Oskarsdottir, J. Catal. 2003, 216, 98-109;.
S. Curtarolo, W. Setyawan, G. L. W. Hart, M. Jahnatek, R. V. Chepulskii, R. H. Taylor, S. Wang, J. Xue, K. Yang, O. Levy, M. J. Mehl, H. T. Stokes, D. O. Demchenko, D. Morgan, Comput. Mater. Sci. 2012, 58, 218-226.
.
J. Behler, J. Chem. Phys. 2016, 145, 170901;.
S. Chmiela, A. Tkatchenko, H. E. Sauceda, I. Poltavsky, K. T. Schütt, K.-R. Müller, Sci. Adv. 2017, 3, e1603015;.
J. P. Janet, C. Duan, T. Yang, A. Nandy, H. J. Kulik, Chem. Sci. 2019, 10, 7913-7922;.
S. Katare, J. M. Caruthers, W. N. Delgass, V. Venkatasubramanian, Ind. Eng. Chem. Res. 2004, 43, 3484-3512;.
A. C. Mater, M. L. Coote, J. Chem. Inf. Model. 2019, 59, 2545-2559.
E. H. Discekici, J. Read de Alaniz, ACS Cent. Sci. 2018, 4, 1087-1088.
Contributed Indexing:: Keywords: materials science; orthogonality; photochemistry; polymer science
Substance Nomenclature:: 0 (Polymers)
Entry Date(s):: Date Created: 20191101 Date Completed: 20210329 Latest Revision: 20210329
Update Code:: 20240104
DOI:: 10.1002/anie.201912001
PMID:: 31667909
: Czasopismo naukowe

Full Text Finder

Selective control of chemical reactions is critical for the proper regulation of processes ranging from intricate biological systems to large scale industrial manufacturing. The progression of synthetic chemistry toward the complexity seen in Nature requires increased control over many concurrent chemical reactions in a non-interfering (orthogonal) fashion. Fortunately, the practically endless pool of synthetic chemical reactions developed to date can often be combined in an orthogonal manner to provide elegant solutions to complex chemical problems. In this review, we first highlight some of the many photochemical reactions that have been applied in orthogonal reaction protocols; the highly selective nature of photochemical reactions makes them well-suited for independent activation in the presence of other reaction components. The application of these orthogonal reactions, especially photochemical reactions, for the synthesis and modification of polymers and polymeric materials is also summarized. Importantly, the use of orthogonal chemical reactions can provide additional opportunities for synthesizing advanced and functional polymeric materials compared to traditional synthetic procedures.
(© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Informacja