-
12
-
-
79953854925
-
-
S. J. Lee K. H. Min H. J. Lee A. N. Koo H. P. Rim B. J. Jeon S. Y. Jeong J. S. Heo S. C. Lee Biomacromolecules 2011 12 1224 1233
-
(2011)
Biomacromolecules
, vol.12
, pp. 1224-1233
-
-
Lee, S.J.1
Min, K.H.2
Lee, H.J.3
Koo, A.N.4
Rim, H.P.5
Jeon, B.J.6
Jeong, S.Y.7
Heo, J.S.8
Lee, S.C.9
-
14
-
-
0037509853
-
-
L. Cao J. A. Massey M. A. Winnik I. Manners S. Riethmüller F. Banhart J. P. Spatz M. Möller Adv. Funct. Mater. 2003 13 271 276
-
(2003)
Adv. Funct. Mater.
, vol.13
, pp. 271-276
-
-
Cao, L.1
Massey, J.A.2
Winnik, M.A.3
Manners, I.4
Riethmüller, S.5
Banhart, F.6
Spatz, J.P.7
Möller, M.8
-
17
-
-
0033639785
-
-
J. P. Spatz S. Mössmer C. Hartmann M. Möller T. Herzog M. Krieger H.-G. Boyen P. Ziemann B. Kabius Langmuir 2000 16 407 415
-
(2000)
Langmuir
, vol.16
, pp. 407-415
-
-
Spatz, J.P.1
Mössmer, S.2
Hartmann, C.3
Möller, M.4
Herzog, T.5
Krieger, M.6
Boyen, H.-G.7
Ziemann, P.8
Kabius, B.9
-
21
-
-
80054993924
-
-
J. B. Gilroy P. A. Rupar G. R. Whittell L. Chabanne N. J. Terrill M. A. Winnik I. Manners R. M. Richardson J. Am. Chem. Soc. 2011 133 17056 17062
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 17056-17062
-
-
Gilroy, J.B.1
Rupar, P.A.2
Whittell, G.R.3
Chabanne, L.4
Terrill, N.J.5
Winnik, M.A.6
Manners, I.7
Richardson, R.M.8
-
23
-
-
77953988899
-
-
J. B. Gilroy T. Gädt G. R. Whittell L. Chabanne J. M. Mitchels R. M. Richardson M. A. Winnik I. Manners Nat. Chem. 2010 2 566 570
-
(2010)
Nat. Chem.
, vol.2
, pp. 566-570
-
-
Gilroy, J.B.1
Gädt, T.2
Whittell, G.R.3
Chabanne, L.4
Mitchels, J.M.5
Richardson, R.M.6
Winnik, M.A.7
Manners, I.8
-
35
-
-
84869454417
-
-
H. Qiu G. Russo P. A. Rupar L. Chabanne M. A. Winnik I. Manners Angew. Chem., Int. Ed. 2012 51 11882 11885
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 11882-11885
-
-
Qiu, H.1
Russo, G.2
Rupar, P.A.3
Chabanne, L.4
Winnik, M.A.5
Manners, I.6
-
43
-
-
11444254100
-
-
H. Tang Y. Liu X. Chen J. Qin M. Inokuchi M. Kinoshita X. Jin Z. Wang B. Xu Macromolecules 2004 37 9785 9792
-
(2004)
Macromolecules
, vol.37
, pp. 9785-9792
-
-
Tang, H.1
Liu, Y.2
Chen, X.3
Qin, J.4
Inokuchi, M.5
Kinoshita, M.6
Jin, X.7
Wang, Z.8
Xu, B.9
-
44
-
-
84863279792
-
-
D. Janczewski J. Song E. Csanyi L. Kiss P. Blazso R. L. Katona M. A. Deli G. Gros J. Xu G. J. Vancso J. Mater. Chem. 2012 22 6429 6435
-
(2012)
J. Mater. Chem.
, vol.22
, pp. 6429-6435
-
-
Janczewski, D.1
Song, J.2
Csanyi, E.3
Kiss, L.4
Blazso, P.5
Katona, R.L.6
Deli, M.A.7
Gros, G.8
Xu, J.9
Vancso, G.J.10
-
46
-
-
0037139588
-
-
M. Ginzburg M. J. MacLachlan S. M. Yang N. Coombs T. W. Coyle N. P. Raju J. E. Greedan R. H. Herber G. A. Ozin I. Manners J. Am. Chem. Soc. 2002 124 2625 2639
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 2625-2639
-
-
Ginzburg, M.1
Maclachlan, M.J.2
Yang, S.M.3
Coombs, N.4
Coyle, T.W.5
Raju, N.P.6
Greedan, J.E.7
Herber, R.H.8
Ozin, G.A.9
Manners, I.10
-
51
-
-
0001616625
-
-
D. L. Zechel K. C. Hultzsch R. Rulkens D. Balaishis Y. Ni J. K. Pudelski A. J. Lough I. Manners D. A. Foucher Organometallics 1996 15 1972 1978
-
(1996)
Organometallics
, vol.15
, pp. 1972-1978
-
-
Zechel, D.L.1
Hultzsch, K.C.2
Rulkens, R.3
Balaishis, D.4
Ni, Y.5
Pudelski, J.K.6
Lough, A.J.7
Manners, I.8
Foucher, D.A.9
-
60
-
-
67649742226
-
-
J. Xu X. Li C. M. Cho C. L. Toh L. Shen K. Y. Mya X. Lu C. He J. Mater. Chem. 2009 19 4740 4745
-
(2009)
J. Mater. Chem.
, vol.19
, pp. 4740-4745
-
-
Xu, J.1
Li, X.2
Cho, C.M.3
Toh, C.L.4
Shen, L.5
Mya, K.Y.6
Lu, X.7
He, C.8
-
61
-
-
79960274979
-
-
Y. Li W.-B. Zhang I. F. Hsieh G. Zhang Y. Cao X. Li C. Wesdemiotis B. Lotz H. Xiong S. Z. D. Cheng J. Am. Chem. Soc. 2011 133 10712 10715
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 10712-10715
-
-
Li, Y.1
Zhang, W.-B.2
Hsieh, I.F.3
Zhang, G.4
Cao, Y.5
Li, X.6
Wesdemiotis, C.7
Lotz, B.8
Xiong, H.9
Cheng, S.Z.D.10
-
62
-
-
84867787164
-
-
Y. Li X.-H. Dong K. Guo Z. Wang Z. Chen C. Wesdemiotis R. P. Quirk W. Zhang S. Z. D. Cheng ACS Macro Lett. 2012 1 834 839
-
(2012)
ACS Macro Lett.
, vol.1
, pp. 834-839
-
-
Li, Y.1
Dong, X.-H.2
Guo, K.3
Wang, Z.4
Chen, Z.5
Wesdemiotis, C.6
Quirk, R.P.7
Zhang, W.8
Cheng, S.Z.D.9
-
69
-
-
64549115297
-
-
39, so for the same amount of radical-induced crosslinking, the former is 16 times as likely to undergo a radical-induced side reaction. In addition, the reactions involving a deficit of thiol also show a greater tendency to afford polymers with these high molecular weight shoulders, which is consistent with a side reaction involving radicals
-
J.-C. Eloi D. A. Rider J.-Y. Wang T. P. Russell I. Manners Macromolecules 2008 41 9474 9479
-
(2008)
Macromolecules
, vol.41
, pp. 9474-9479
-
-
Eloi, J.-C.1
Rider, D.A.2
Wang, J.-Y.3
Russell, T.P.4
Manners, I.5
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