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KF?Silica as a stationary phase for the chromatographic removal of tin residues from organic compoundsElectronic supplementary information (ESI) available: uncropped images of the spectra presented in Figs. 1a?d. See http://www.rsc.org/suppdata/cc/b4/b406041e/

✍ Scribed by Harrowven, David C.; Guy, Ian L.

Book ID: 111650687
Publisher: Royal Society of Chemistry
Year: 2004
Tongue: English
Weight: 100 KB
Volume: 17
Category: Article
ISSN: 1359-7345
DOI: 10.1039/b406041e

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📜 SIMILAR VOLUMES

Complementary hydrogen bonding in a new

Complementary hydrogen bonding in a new tridentate Schiff base ligand: X-ray, DFT and solution NMR studiesElectronic supplementary information (ESI) available: unit cell packing diagram for 3 (Fig. S1) and 1H NMR spectra of 3 as a function of the concentration of added H2O in CDCl3 solution (Fig. S2). See http://www.rsc.org/suppdata/nj/b3/b305946d/

✍ Munro, Orde Q.; Strydom, Sandra D.; Grimmer, Craig D. 📂 Article 📅 2004 🏛 Royal Society of Chemistry 🌐 English ⚖ 605 KB

The Hendrickson reagent and the Mitsunob

The Hendrickson reagent and the Mitsunobu reaction: a mechanistic studyElectronic supplementary information (ESI) available: (1) 1H and 13C NMR spectra of 4-chlorobenzyl thioacetate 3 and 4-chlorobenzyl azide 4. (2) 1H NMR stack spectra of alkene region of menthenes 5a?5b formed by (a) thermolysis of menthol diphenylphosphate ester;21 (b) Mitsunobu reagents (Organic Syntheses conditions);16 (c) Hendrickson reagent (Table 1, entry 3) and (d) Hendrickson reagent (Table 1, entry 8). (3) 31P spectra of Mitsunobu reactions performed in the presence of (a) diisopropylethylammonium triflate; (b) diisopropylethylammonium triflate and diisopropylethylamine (2 eq.) and (c) tetrabutylammonium triflate. (4) 1H and 1H{31P} NMR spectra of (?)-menthoxytriphenylphosphonium triflate 11, H3. (5) Table 2 ? raw data for Fig. 3. See http://www.rsc.org/suppdata/ob/b3/b305375j/

✍ Elson, Kathryn E.; Jenkins, Ian D.; Loughlin, Wendy A. 📂 Article 📅 2003 🏛 Royal Society of Chemistry 🌐 English ⚖ 169 KB

Mesoporous silica with Ia3d cubic struct

Mesoporous silica with Ia3d cubic structure and good thermal stabilityElectronic Supplementary Information (ESI) available: XRD and N2 sorption isotherms of the as-synthesized powders calcined in air at 900 �C for 4 h, and the as-synthesized powders calcined in air at 500 �C for 6 h and then calcined in air or nitrogen at 900 �C for 4 h; XRD of the as-synthesized powders when the molar ratio of DM?CTAB is 1?2; EDS spectrum and TGA curve of the powders carbonized in nitrogen at 900 �C for 4 h; proposed formation mechanism of the Ia3d cubic mesostructure in nitrogen at high temperatures such as 900 �C. See http://www.rsc.org/suppdata/cc/b3/b316501a/

✍ Pang, Jiebin; Eric Hampsey, J.; Hu, Qingyuan; Wu, Zhiwang; John, Vijay T.; Lu, Y 📂 Article 📅 2004 🏛 Royal Society of Chemistry 🌐 English ⚖ 221 KB