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0001205090
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PCT Int. Appl. WO 9801478 A1 980115
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Le, T. P.; Moad, G.; Rizzardo, E.; Thang, S. H. PCT Int. Appl. WO 9801478 A1 980115; Chem. Abstr. 1998 128, 115390.
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Le, T.P.1
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2
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0005119939
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PCT Int. Appl. WO 9931144 A1 990624
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Chiefari, J.; Mayadunne, R. T. A.; Moad, G.; Rizzardo, E.; Thang, S. H. PCT Int. Appl. WO 9931144 A1 990624; Chem. Abstr. 1999 131, 45250.
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Moad, G.3
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3
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85069105528
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note
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2CN are examples of very poor and very good homolytic leaving groups, respectively.
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4
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0032135925
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Chiefari, J.; Chong, Y. K.; Ercole, F.; Krstina, J.; Jeffery, J.; Le, T. P. T.; Mayadunne, R. T. A.; Meijs, G. F.; Moad, C. L.; Moad, G.; Rizzardo, E.; Thang, S. H. Macromolecules 1998, 31, 5559-5562.
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Ercole, F.3
Krstina, J.4
Jeffery, J.5
Le, T.P.T.6
Mayadunne, R.T.A.7
Meijs, G.F.8
Moad, C.L.9
Moad, G.10
Rizzardo, E.11
Thang, S.H.12
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5
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0033406519
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Rizzardo, E.; Chiefari, J.; Chong, Y. K.; Ercole, F.; Krstina, J.; Jeffery, J.; Le, T. P. T.; Mayadunne, R. T. A.; Meijs, G. F.; Moad, C. L.; Moad, G.; Thang, S. H. Macromol. Symp. 1999, 143, 291-307.
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Macromol. Symp.
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Rizzardo, E.1
Chiefari, J.2
Chong, Y.K.3
Ercole, F.4
Krstina, J.5
Jeffery, J.6
Le, T.P.T.7
Mayadunne, R.T.A.8
Meijs, G.F.9
Moad, C.L.10
Moad, G.11
Thang, S.H.12
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6
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0032624512
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Rizzardo, E.; Chiefari, J.; Moad, G.; Mayadunne, R. T. A.; Thang, S. H. Polym. Prepr. 1999, 40, 342-343.
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Polym. Prepr.
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Moad, G.3
Mayadunne, R.T.A.4
Thang, S.H.5
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7
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0033204692
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Mayadunne, R. T. A.; Rizzardo, E.; Chiefari, J.; Chong, Y. K.; Moad, G.; Thang, S. H. Macromolecules 1999, 32, 6977-6980.
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Macromolecules
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Mayadunne, R.T.A.1
Rizzardo, E.2
Chiefari, J.3
Chong, Y.K.4
Moad, G.5
Thang, S.H.6
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8
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13044256394
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Chong, Y. K.; Le, T. P.; Moad, G.; Rizzardo, E.; Thang, S. H. Macromolecules 1999, 32, 2071-2074.
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Chong, Y.K.1
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Thang, S.H.5
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12
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0002585959
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Salamone, J. C., Ed.; CRC Press: Boca Raton, FL
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Rizzardo, E.; Moad, G. In The Polymeric Materials Encyclopaedia: Synthesis, Properties and Applications; Salamone, J. C., Ed.; CRC Press: Boca Raton, FL, 1996; Vol. 5, p 3834.
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Rizzardo, E.1
Moad, G.2
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13
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85069095889
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note
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8 The advantage of trithiocarbonates is that they are more readily available.
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14
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0001620539
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For leading references on the reactions of dithio compounds, see: Kato, S.; Ishida, M. Sulfur Rep. 1988, 8, 155. Mayer, R.; Scheithauer, S. In Houben-Weyl Methods of Organic Chemistry; Beuchel, K. H., Falbe, J., Hagemann, H., Hanack, M., Eds.; Thieme: Stuttgart, Germany, 1985; Vol. E, p 891.
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Sulfur Rep.
, vol.8
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Kato, S.1
Ishida, M.2
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15
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0000270662
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Beuchel, K. H., Falbe, J., Hagemann, H., Hanack, M., Eds.; Thieme: Stuttgart, Germany
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For leading references on the reactions of dithio compounds, see: Kato, S.; Ishida, M. Sulfur Rep. 1988, 8, 155. Mayer, R.; Scheithauer, S. In Houben-Weyl Methods of Organic Chemistry; Beuchel, K. H., Falbe, J., Hagemann, H., Hanack, M., Eds.; Thieme: Stuttgart, Germany, 1985; Vol. E, p 891.
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Houben-Weyl Methods of Organic Chemistry
, vol.E
, pp. 891
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Mayer, R.1
Scheithauer, S.2
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16
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0000822930
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Lee, A. W. M.; Chan, W. H.; Wong, H. C. Synth. Commun. 1988, 18, 1531-1536.
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Synth. Commun.
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Lee, A.W.M.1
Chan, W.H.2
Wong, H.C.3
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84955629620
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PCT Int. Appl. WO 9905099 A1 990204
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Moad, G.; Rizzardo, E.; Thang, S. H. PCT Int. Appl. WO 9905099 A1 990204; Chem. Abstr. 1999 130, 154069. Thang, S. H.; Chong, Y. K.; Mayadunne, R. T. A.; Moad, G.; Rizzardo, E. Tetrahedron Lett. 1999, 40, 2435-2438.
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Chem. Abstr.
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Moad, G.1
Rizzardo, E.2
Thang, S.H.3
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18
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0033583148
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Moad, G.; Rizzardo, E.; Thang, S. H. PCT Int. Appl. WO 9905099 A1 990204; Chem. Abstr. 1999 130, 154069. Thang, S. H.; Chong, Y. K.; Mayadunne, R. T. A.; Moad, G.; Rizzardo, E. Tetrahedron Lett. 1999, 40, 2435-2438.
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Tetrahedron Lett.
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Thang, S.H.1
Chong, Y.K.2
Mayadunne, R.T.A.3
Moad, G.4
Rizzardo, E.5
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19
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85069092041
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note
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As described in our previous publications, the amount of impurity polymer (homo- and diblock impurity) produced is dependent on the number of initiator-derived chains and not the amount of initiator used in the experiment. In ascertaining the amount of initiator derived chains, based on the rate of decomposition of the initiator, allowance must also be made for the efficiency of the initiator. Thus, in summary: [initiator-derived chains] = [initiator decomposed] × [initiator efficiency] × 2 = [diblock impurity] + [homopolymer impurity].
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