MOESM1 of Magnetic γFe2O3@Sh@Cu2O: an efficient solid-phase catalyst for reducing agent and base-free click synthesis of 1,4-disubstituted-1,2,3-triazoles

2020-01-08T04:56:50Z (GMT) by Fereshteh Norouzi Shahrzad Javanshir
Additional file 1. Figure S1. 1HNMR of 1-(4-bromobenzyl)-4-(4-methoxyphenyl)-1,2,3-triazole. Figure S2. Expanded 1HNMR spectra of 1-(4-bromobenzyl)-4-(4-methoxyphenyl)-1,2,3-triazole (aromatic region). Figure S3. 13CNMR of 1-(4-bromobenzyl)-4-(4-methoxyphenyl)-1,2,3-triazole. Figure S4. 13CNMR of 1-(4-bromobenzyl)-4-(4-methoxyphenyl)-1,2,3-triazole. Figure S5. 1HNMR of 1-(2-chlorobenzyl)-4-(4-methoxyphenyl)-1H-1,2,3-triazole. Figure S6. Expanded 1HNMR spectra of 1-(2-chlorobenzyl)-4-(4-methoxyphenyl)-1H-1,2,3-triazole (aromatic region). Figure S7. 13CNMR of 1-(2-chlorobenzyl)-4-(4-methoxyphenyl)-1H-1,2,3-triazole. Figure S8. Expanded 13CNMR spectra of 1-(2-chlorobenzyl)-4-(4-methoxyphenyl)-1H-1,2,3-triazole. Figure S9. 1HNMR of 1-(2-chlorobenzyl)-4-(4-p-tolyl)-1H-1,2,3-triazole. Figure S10. Expanded 1HNMR spectra of 1-(2-chlorobenzyl)-4-(p-tolyl)-1H-1,2,3-triazole (aromatic region). Figure S11. 13CNMR of 1-(2-chlorobenzyl)-4-(p-tolyl)-1H-1,2,3-triazole. Figure S12. Expanded 13CNMR spectra of 1-(2-chlorobenzyl)-4-(p-tolyl)-1H-1,2,3-triazole.