Squaric Acid Mediated Bioconjugation Expanded to Polymers ... · 1 Electronic Supplementary...
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Electronic Supplementary Information for:
Squaric Acid Mediated Bioconjugation
Expanded to Polymers Prepared by ATRP
Tobias Steinbach, Frederik Wurm and Harm-Anton Klok*
Ecole Polytechnique Fédérale de Lausanne (EPFL), Institut des Matériaux and Institut des
Sciences et Ingénierie Chimiques, Laboratoire des Polymères, Bâtiment MXD, Station 12,
CH-1015 Lausanne, Switzerland.
* Corresponding author: Fax: + 41 21 693 5650; Tel: + 41 21 693 4866; E-mail: [email protected]
Electronic Supplementary Material (ESI) for Polymer Chemistry.This journal is © The Royal Society of Chemistry 2014
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Figure S1: 1H NMR spectrum of 3-ethoxy-4-(2-hydroxyethylamino)cyclobut-3-ene-1,2-dione (1) in DMSO-d6.
Figure S2: 1H NMR spectrum of 2-(2-ethoxy-3,4-dioxocyclobut-1-enylamino)ethyl 2-bromo-2-methylpropanoate (2) in DMSO-d6.
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Figure S3: 13C NMR spectrum of 2-(2-ethoxy-3,4-dioxocyclobut-1-enylamino)ethyl 2-bromo-2-methylpropanoate (2) in DMSO-d6.
200 300 400 500 600 700 800
O O
O NH
O
O
Br 2MH+
MK+
m/z
334
374
668
MH+
Figure S4: ESI mass spectrum of 2-(2-ethoxy-3,4-dioxocyclobut-1-enylamino)ethyl 2-bromo-2-methylpropanoate (2).
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Figure S5: 1H NMR spectrum of 3-(1,3-dihydroxypropan-2-ylamino)-4-ethoxycyclobut-3-ene-1,2-dione (3) in DMSO-d6.
Figure S6: 13C NMR of 3-(1,3-dihydroxypropan-2-ylamino)-4-ethoxycyclobut-3-ene-1,2-dione (3) in DMSO-d6.
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Figure S7: 1H NMR spectrum of 2-(2-ethoxy-3,4-dioxocyclobut-1-enylamino)propane-1,3-diyl bis(2-bromo-2-methylpropanoate) (4) in CDCl3.
Figure S8: 13C NMR spectrum of 2-(2-ethoxy-3,4-dioxocyclobut-1-enylamino)propane-1,3-diyl bis(2-bromo-2-methylpropanoate) (4) in CDCl3.
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Figure S9: ESI mass spectrum of 2-(2-ethoxy-3,4-dioxocyclobut-1-enylamino)propane-1,3-diyl bis(2-bromo-2-methylpropanoate) (4).
Figure S10: 1H NMR spectrum of 3-(1,3-dihydroxy-2-(hydroxymethyl)propan-2-ylamino)-4-ethoxycyclobut-3-ene-1,2-dione (5) in DMSO-d6.
MH+
MK+
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Figure S11: 13C NMR spectrum of 3-(1,3-dihydroxy-2-(hydroxymethyl)propan-2-ylamino)-4-ethoxycyclobut-3-ene-1,2-dione (5) in DMSO-d6.
Figure S12: 1H NMR spectrum of 2-((2-bromo-2-methylpropanoyloxy)methyl)-2-(2-ethoxy-3,4-dioxocyclobut-1-enylamino)propane-1,3-diyl bis(2-bromo-2-methylpropanoate) (6) in CDCl3.
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Figure S13: 13C NMR spectrum of 2-((2-bromo-2-methylpropanoyloxy)methyl)-2-(2-ethoxy-3,4-dioxocyclobut-1-enylamino)propane-1,3-diyl bis(2-bromo-2-methylpropanoate) (6) in CDCl3.
Figure S14: ESI mass spectrum of 2-((2-bromo-2-methylpropanoyloxy)methyl)-2-(2-ethoxy-3,4-dioxocyclobut-1-enylamino)propane-1,3-diyl bis(2-bromo-2-methylpropanoate) (6).
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Figure S15: 1H NMR spectrum of mid-functionalized PPEGMA # 2 in CDCl3.
Figure S16: 1H NMR spectrum of three-arm PPEGMA #6 in CDCl3.
