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Cation????? interactions as a tool to enhance the power of a chiral auxiliary during asymmetric photoreactions within zeolitesElectronic supplementary information (ESI) available: HF/3-21G optimized structures of Li+ bound 3a and 3c, Na+ bound 5a and 5c and enlarged Fig. 1. See http://www.rsc.org/suppdata/cc/b2/b209810e/

✍ Scribed by Kaanumalle, Lakshmi S.; Sivaguru, J.; Arunkumar, N.; Karthikeyan, S.; Ramamurthy, V.

Book ID: 120168650
Publisher: Royal Society of Chemistry
Year: 2003
Tongue: English
Weight: 293 KB
Volume: 1
Category: Article
ISSN: 1359-7345
DOI: 10.1039/B209810E

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📜 SIMILAR VOLUMES

Physical stability vs. chemical lability

Physical stability vs. chemical lability in microporous metal coordination polymers: a comparison of [Cu(OH)(INA)]n and [Cu(INA)2]n: INA = 1,4-(NC5H4CO2)Electronic supplementary information (ESI) available: 1. Structure determination summaries for compounds 1–3. 2. Powder X-ray diffraction patterns: (a) for 1 and (b) for 2 after prolonged heating at different temperatures, establishing framework stabilities and (c) showing transformation of polymer 2 to the molecular compound 3, after 12 h in H2O. Fig. S1: copper coordination environments in compounds 1–3. See http://www.rsc.org/suppdata/cc/b2/b201501n/

✍ Lin, Candy Z-J.; Chui, Stephen S-Y.; Lo, Samuel M-F.; Shek, Fanny L-Y.; Wu, Ming 📂 Article 📅 2002 🏛 Royal Society of Chemistry 🌐 English ⚖ 149 KB

1H-1,3-Diazepines, 5H-1,3-diazepines, 1,

1H-1,3-Diazepines, 5H-1,3-diazepines, 1,3-diazepinones, and 2,4-diazabicyclo[3.2.0]heptenesPreliminary reports on parts of this work have been published in ref 1. This paper is Diazepines, Part 3. For Part 2, see ref 2.,Electronic supplementary information (ESI) available: NMR spectra of 4a, 4c, 19v ? 20, 19a ? 25a, and 19g ? 25g (Fig. S1?S6), Arrhenius and Eyring plots for H-exchange in 4b,c (Fig. S7), views of the X-ray crystal structures of compounds 26 and 22bB (Fig. S8?S9), bond lengths and angles for compounds 4k, 22bB and 26, preparative procedures and characterization data for all compounds not described in the Experimental section, and computational data (Cartesian coordinates, absolute energies, IR, 1H and 13C NMR) for 20a?c, 21a?b, 22aA?F and 22aB dimer. See http://www.rsc.org/suppdata/ob/b3/b317099c/

✍ Reisinger, Ales; Koch, Rainer; Bernhardt, Paul V.; Wentrup, Curt 📂 Article 📅 2004 🏛 Royal Society of Chemistry 🌐 English ⚖ 496 KB