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Books on the topic 'Calixareni'

Author: Grafiati

Published: 10 March 2023

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1

Gutsche, C. David. Calixarenes. Cambridge: Royal Society of Chemistry, 1992.

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2

Asfari, Zouhair, Volker Böhmer, Jack Harrowfield, Jacques Vicens, and Mohamed Saadioui, eds. Calixarenes 2001. Dordrecht: Kluwer Academic Publishers, 2002. http://dx.doi.org/10.1007/0-306-47522-7.

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3

Calixarenes revisited. Cambridge: Royal Society of Chemistry, 1998.

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4

Z, Asfari, ed. Calixarenes 2001. Dordrecht: Kluwer Academic Publishers, 2001.

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5

Z, Asfari, ed. Calixarenes 2001. Dordrecht: Kluwer Academic Publishers, 2001.

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6

Surov, O. V. Calixarene complexes with solvent molecules. New York: Nova Science Publishers, 2010.

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7

Neri, Placido, Jonathan L. Sessler, and Mei-Xiang Wang, eds. Calixarenes and Beyond. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31867-7.

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8

Lumetta, Gregg J., Robin D. Rogers, and Aravamudan S. Gopalan, eds. Calixarenes for Separations. Washington, DC: American Chemical Society, 2000. http://dx.doi.org/10.1021/bk-2000-0757.

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9

Luigi, Mandolini, and Ungaro Rocco, eds. Calixarenes in action. London: Imperial College Press, 2000.

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10

Royal Society of Chemistry (Great Britain), ed. Calixarenes: An introduction. 2nd ed. Cambridge: RSC Pub., 2008.

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11

J, Vicens, and Böhmer V, eds. Calixarenes: A versatile class of macrocyclic compounds. Dordrecht: Kluwer Academic Publishers, 1991.

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12

J, Vicens, Asfari Z, and Harrowfield J. M, eds. Calixarenes 50th anniversary: Commemorative issue. Dordrecht: Kluwer Academic, 1995.

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13

Vicens, J., Z. Asfari, and J. M. Harrowfield, eds. Calixarenes 50th Anniversary: Commemorative Issue. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0267-4.

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14

Vicens, J. Calixarenes 50th Anniversary: Commemorative Issue. Dordrecht: Springer Netherlands, 1995.

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15

Deska, M. Covalently and noncovalently bound assemblies of calixarenes. Hauppauge, N.Y: Nova Science Publishers, 2011.

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16

Deska, M. Covalently and noncovalently bound assemblies of calixarenes. Hauppauge, N.Y: Nova Science Publishers, 2010.

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17

Vicens, J., and V. Böhmer, eds. Calixarenes: A Versatile Class of Macrocyclic Compounds. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-2013-2.

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18

Petters, Dean David. Calixarene derivatives as templates in the synthesis of novel metal clusters. Birmingham: University of Birmingham, 1995.

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19

Martin, Jonathan Paul. The synthesis and evaluation of calixarene hydrophobic hosts designed to recognise small organic molecules. Birmingham: University of Birmingham, 1991.

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20

Cornejo, Adolfo F. A. Solution and solid state studies of metal complexes of some EDTA and calixarene derivatives. Dublin: University College Dublin, 1998.

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21

Goodsell, David S. Bionanotechnology. New York: John Wiley & Sons, Ltd., 2004.

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22

Calixarenes. Cambridge: Royal Society of Chemistry, 2008. http://dx.doi.org/10.1039/9781847558190.

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23

Calixarenes Revisited. Cambridge: Royal Society of Chemistry, 1998. http://dx.doi.org/10.1039/9781847550293.

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24

Asfari, M. Z., Volker Böhmer, Jacques Vicens, and J. Harrowfield. Calixarenes 2001. Springer London, Limited, 2007.

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25

(Editor), M. Z. Asfari, Volker Böhmer (Editor), J. Harrowfield (Editor), and J. Vicens (Editor), eds. Calixarenes 2001. Springer, 2001.

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26

Asfari, M. Z., Volker Böhmer, Jacques Vicens, and J. Harrowfield. Calixarenes 2001. Springer Netherlands, 2010.

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27

Sessler, Jonathan L., Placido Neri, and Mei-Xiang Wang. Calixarenes and Beyond. Springer, 2018.

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28

Mandolini, Luigi, and Rocco Ungaro. Calixarenes in Action. PUBLISHED BY IMPERIAL COLLEGE PRESS AND DISTRIBUTED BY WORLD SCIENTIFIC PUBLISHING CO., 2000. http://dx.doi.org/10.1142/p168.

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29

1960-, Lumetta Gregg J., Rogers Robin D, and Gopalan Aravamudan S. 1954-, eds. Calixarenes for separations. Washington, DC: American Chemical Society, 2000.

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30

Sessler, Jonathan L., Placido Neri, and Mei-Xiang Wang. Calixarenes and Beyond. Springer London, Limited, 2016.

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31

Sessler, Jonathan L., Placido Neri, and Mei-Xiang Wang. Calixarenes and Beyond. Springer, 2016.

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32

Calixarene Complexes: Synthesis, Properties and Applications. MDPI, 2021. http://dx.doi.org/10.3390/books978-3-0365-1634-9.

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33

Vicens, Jacques, Jack Harrowfield, and Lassaad Baklouti, eds. Calixarenes in the Nanoworld. Springer Netherlands, 2007. http://dx.doi.org/10.1007/978-1-4020-5022-4.

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34

(Assistant), L. Baklouit, Jacques Vicens (Editor), and Jack Harrowfield (Editor), eds. Calixarenes in the Nanoworld. Springer, 2006.

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35

Vicens, Jacques, Jack Harrowfield, and L. Baklouit. Calixarenes in the Nanoworld. Springer, 2010.

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36

Vicens, Jacques, Jack Harrowfield, and L. Baklouit. Calixarenes in the Nanoworld. Springer London, Limited, 2006.

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37

Calixarenes 50th Anniversary: Commemorative Issue. Springer, 1995.

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38

Vicens, Jacques, M. Z. Asfari, and J. Harrowfield. Calixarenes 50th Anniversary: Commemorative Issue. Springer, 2012.

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39

(Editor), J. Vicens, and Volker Böhmer (Editor), eds. Calixarenes, a Versatile Class of Macrocyclic Compounds (Topics in Inclusion Science) (Topics in Inclusion Science). Springer, 1990.

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40

Böhmer, Volker, and Jacques Vicens. Calixarenes: A Versatile Class of Macrocyclic Compounds. Springer, 2012.

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41

GUTSCHE, C. MSC: CALIXARENES REVISITED (Monographs in Supramolecular Chemistry). Royal Society of Chemistry, 1998.

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42

Calixarenes and Resorcinarenes: Synthesis, Properties and Applications. Wiley & Sons, Limited, John, 2009.

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43

Calixarenes H/C (Monographs in Supramolecular Chemistry). Royal Society of Chemistry, 1989.

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44

Vicens, Jacques. Calixarenes: A Versatile Class of Macrocyclic Compounds. Springer, 2011.

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45

Desai, Bimbisar. Tubular molecules derived from calixarenes and their complexation studies. 2000.

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46

Mareeswaran, Paulpandian Muthu, Palaniswamy Suresh, and Seenivasan Rajagopal, eds. Photophysics of Supramolecular Architectures. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/97898150491901220101.

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Abstract:

This reference provides collective information about the physical and photophysical changes of supramolecules after encapsulation. It covers luminescent systems involving a range of host molecules such as calixarenes, cyclodextrin, resorcinanene-crowns, pillararenes, cucurbituril, and metallacycles. Chapters also discuss the effect of the macrocyclic environment on the properties of functionalized molecules, including the variations in folding and unfolding patterns. Each chapter is supplemented with detailed references, making this an ideal resource for scholars interested in supramolecular photophysics.

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47

New Macrocyclic Extractants For Radioactive Waste Treatment: Ionizable Crown Ethers And Functionalized Calixarenes Eur 17615. Commission of the European, 1997.

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48

Goodsell, David S. Bionanotechnology: Lessons from Nature. Wiley & Sons, Incorporated, John, 2004.

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49

Goodsell, David S. Bionanotechnology: Lessons from Nature. Wiley & Sons, Incorporated, John, 2007.

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50

Bionanotechnology: Lessons from Nature. Wiley-Liss, 2004.

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