Calixarenes and Beyond - download pdf or read online

By Placido Neri, Jonathan L. Sessler, Mei-Xiang Wang

ISBN-10: 3319318659

ISBN-13: 9783319318653

ISBN-10: 3319318675

ISBN-13: 9783319318677

Contributions that includes the chemistry and purposes of a family members of macrocyclic compounds jointly often called 'calixarenes' are awarded during this edited quantity. The arsenal of constructions in keeping with calixarenes presents instruments that are potent in different components of supramolecular chemistry. The Editors have compiled a well timed quantity which incorporates modern, excessive calibre contributions from a lot of overseas authors. A wide point of view at the development and way forward for calixarene chemistry is gifted. aimed toward scholars and researchers energetic in Supramolecular Chemistry.

Show description

Read Online or Download Calixarenes and Beyond PDF

Best inorganic books

The Organometallic Chemistry of the Transition Metals, by Robert H. Crabtree PDF

Absolutely up to date and improved to mirror fresh advances, this Fourth version of the vintage textual content presents scholars chemists with an exceptional advent to the rules and normal homes of organometallic compounds, in addition to together with functional info on response mechanisms and specified descriptions of latest purposes.

Download e-book for iPad: The Organic Chemistry of Nickel. Organic Synthesis by P.W. Jolly (Auth.)

The natural Chemistry of Nickel summary: The natural Chemistry of Nickel

Inorganic Molecules by G. Graner, E. Hirota, T. Iijima, K. Kuchitsu, D. A. Ramsay, PDF

Quantity II/25 is a supplemented and revised version of the previous volumes II/7, II/15, II/21 and II/23 containing brand new details on inorganic and natural polyatomic molecules. All experimental tools for the selection of quantitative structural facts of loose molecules were thought of: microwave, infrared, Raman, digital and photoelectron spectroscopy in addition to electron diffraction.

Extra resources for Calixarenes and Beyond

Example text

104. ; B€ohmer, V. Supramol. Chem. 2010, 22, 717–725. 105. ; Vysotsky, M. ; Bohmer, V. Chem. Commun. 2003, 1124–1125. 106. ; Zheng, Y. S. Curr. Org. Chem. 2012, 16, 483–506. 107. ; Reinhoudt, D. N. Supramol. Chem. 2007, 19, 95–106. 108. Prins, L. ; Reinhoudt, D. N. Nature 1999, 398, 498–502. 109. ; Reinhoudt, D. ; Shinkai, S. Angew. Chem. Int. Ed. 2002, 41, 1924–1929. 110. ; Reinhoudt, D. ; Shinkai, S. J. Am. Chem. Soc. 2002, 124, 14631–14641. 1 Foreword One of the main advantages of the chemistry of calixarenes is the fact that they can be, with only few limitations, easily derivatised by numerous functional groups.

Zhang, C. Org. Lett. 2004, 6, 1189–1192. 44. Liu, X. ; Zheng, Y. S. Tetrahedron Lett. 2006, 47, 6357–6360. 45. ; Sirit, A. Tetrahedron: Asymmetry 2008, 19, 618–623. 46. ; Jabin, I. Tetrahedron: Asymmetry 2005, 16, 3767–3771. 47. ; Jabin, I. J. Org. Chem. 2005, 70, 10552–10560. 48. Wezenberg, S. ; Kleij, A. W. Adv. Synth. Catal. 2010, 352, 85–91. 49. Amato, M. ; Ballistreri, F. ; Tomaselli, G. ; Toscano, R. ; Williams, D. J. Eur. J. Org. Chem. 2005, 3562–3570. 50. ; Ungaro, R. J. Org. Chem. 1997, 62, 8654–8659.

However, the complexation process is hedged by a high kinetic barrier. Therefore, complexation of fullerenes can only be realized at the step of capsule formation (during chemical reaction) or, by pushing fullerenes into capsules by mechanochemical methods. Interestingly, the chiral cavity has a profound effect on the 13C NMR spectrum of fullerene C70. Enantiotopic carbon atoms became diastereotopic in the chiral environment and therefore exhibited different chemical shifts. 2 Chiral Calixarenes and Resorcinarenes 21 Fig.

Download PDF sample

Calixarenes and Beyond by Placido Neri, Jonathan L. Sessler, Mei-Xiang Wang


by Robert
4.3

Rated 4.53 of 5 – based on 43 votes