“…H NMR (400 MHz, CDCl 3 ): δ (ppm)6.54 (q, 8H, −CH (allyl)), 5.27−5.18 (q, 16H, −CHCH 2 (allyl)), 5.27−5.18 (q, 16H, CH 2 −O (allyl)), 4.21 (q, 12H, −CH 2 −OCO− (bis-MPA)), 3.31 (s, 1828H, CH 2 −CH 2 −O− (PEG)), 2.60 (q, 64H, CH 2 −CHCH 2 (allyl)), 1.20−1.09 (q, 18H, −CH 3 (Bis-MPA)) 13. C NMR (100 MHz, CDCl 3 ): δ (ppm) 172.3 (1C, −COO− (allyl)), 172 (1C, −COO− (bis-MPA, allyl)), 138.3 (1C, −C (allyl)), 117.6 (1C, CH 2 (allyl)), 72.3 (1C, −CH 2 −O (allyl)), 70.75 (2C, −CH 2 − CH 2 −O (PEG)), 68.0−64.1 (1C, −CH 2 −O (bis-MPA)), 50.2 (1C, −COO−C−((CH 2 −OH) 2 , CH 3 ) (bis-MPA)), 49.5 (1C, −COOH− C−((CH 2 −OR) 2 , CH 3 ) (bis-MPA)), 48.1 (1C, −COO−C−(CH 2 − OH, CH 3 , CH 2 −OR) (bis−MPA)), 46.2, 45.5 (1C,−COO−C− ((CH 2 −OR) 2 , CH 3 ) (bis-MPA)), 29.7 (1C, −CH 2 −CC (allyl)), 29.0 (1C, −CH 2 −COO (allyl)) 17.8 (1C, −CH 3 (bis-MPA)).…”