Pyridyl Conjugated 1,2,3-Triazole is a Versatile Coordination Ability Ligand Enabling Supramolecular Associations

Damijana Urankar; Andrej Pevec; Iztok Turel; Janez Košmrlj

doi:10.1021/cg100993k

journal article Oct 04, 2010

Pyridyl Conjugated 1,2,3-Triazole is a Versatile Coordination Ability Ligand Enabling Supramolecular Associations

Damijana Urankar Andrej Pevec Iztok Turel

Janez Košmrlj

Crystal Growth & Design Vol. 10 No. 11 pp. 4920-4927 · American Chemical Society (ACS)

View at Publisher Save 10.1021/cg100993k

Topics

No keywords indexed for this article. Browse by subject →

References

45

[1]

Kickelbick G. (2007)

[2]

Desiraju G. R. Science (1997) 10.1126/science.278.5337.404

[3]

Huisgen, R.In1,3-Dipolar Cycloaddition Chemistry;Padwa, A., Ed.Wiley:New York, 1984; Vol.1, pp1−176.

[4]

Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

Christian W. Tornøe, Caspar Christensen, Morten Meldal

The Journal of Organic Chemistry 2002 10.1021/jo011148j

[5]

Rostovtsev V. V. Angew. Chem., Int. Ed. (2002) 10.1002/1521-3773(20020715)41:14<2596::aid-anie2596>3.0.co;2-4

[6]

Mindt T. L. J. Am. Chem. Soc. (2006) 10.1021/ja066779f

[7]

Struthers H. Dalton. Trans. (2010) 10.1039/b912608b

[8]

Brotherton W. S. Org. Lett. (2009) 10.1021/ol9021113

[9]

Crowley J. D. Polyhedron (2010) 10.1016/j.poly.2009.06.010

[10]

Fu Y. Chin. J. Inorg. Chem. (2010)

[11]

Urankar D. Inorg. Chem. (2010) 10.1021/ic902354e

[12]

Kuang G.-C. J. Org. Chem. (2010) 10.1021/jo101305m

[13]

Bai S.-Q. Cryst. Growth Des. (2010) 10.1021/cg901327m

[14]

Crowley J. D. Dalton Trans. (2010) 10.1039/b911276f

[15]

Bai S.-Q. Dalton Trans. (2010) 10.1039/b918223c

[16]

Cotton F. A. Inorg. Chem. (1980) 10.1021/ic50204a010

[17]

[20] Processing of X-ray diffraction data collected in oscillation mode

Zbyszek Otwinowski, Wladek Minor

Methods in Enzymology 1970 10.1016/s0076-6879(97)76066-x

[18]

Altomare A. J. Appl. Crystallogr. (1993) 10.1107/s0021889892010331

[19]

Sheldrick, G. M.SHELXL97 - Program for Crystal Structure Analysis (Release 97−2);Institut für Anorganische Chemie der Universität:Göttingen, Germany, 1998.

[20]

Chifotides H. T. Acc. Chem. Res. (2005) 10.1021/ar0302078

[21]

Cotton F. A. Inorg. Chem. (1999) 10.1021/ic990618d

[22]

Boyar E. B. Coord. Chem. Rev. (1983) 10.1016/0010-8545(83)85028-0

[23]

Christop G. G. J. Am. Chem. Soc. (1979) 10.1021/ja00500a011

[24]

Yoshimura T. Inorg. Chem. (2003) 10.1021/ic030093w

[25]

Crowley J. D. Dalton Trans. (2010) 10.1039/c003683h

[26]

Schweinfurth D. Dalton Trans. (2009) 10.1039/b910660j

[27]

Badèche S. Inorg. Chem. (2008) 10.1021/ic8002405

[28]

Suijkerbuijk B. M. J. B. Dalton Trans. (2007) 10.1039/b701978p

[29]

Aragay G. J. Organomet. Chem. (2008) 10.1016/j.jorganchem.2008.07.038

[30]

Lee H. M. J. Organomet. Chem. (2005) 10.1016/j.jorganchem.2004.09.053

[31]

Janiak C. J. Chem. Soc., Dalton Trans. (2000) 10.1039/b003010o

[32]

Hunter C. A. J. Am. Chem. Soc. (1990) 10.1021/ja00170a016

[33]

Zhang X. Inorg. Chem. Commun. (2003) 10.1016/j.inoche.2003.08.013

[34]

Bortoluzzi M. Polyhedron (2010) 10.1016/j.poly.2009.10.025

[35]

Amine−Amide Equilibrium in Gold(III) Complexes and a Gold(III)−Gold(I) Aurophilic Bond

Michael C. Jennings, Richard J. Puddephatt

Inorganic Chemistry 2007 10.1021/ic061911y

[36]

Kilpin K. J. Inorg. Chim. Acta (2010) 10.1016/j.ica.2009.10.003

[37]

Segapelo T. V. Inorg. Chim. Acta (2009) 10.1016/j.ica.2009.02.046

[38]

Mohamed A. A. Coord. Chem. Rev. (2010) 10.1016/j.ccr.2010.02.003

[39]

Eryazici I. Chem. Rev. (2008) 10.1021/cr0781059

[40]

Khavasi H. R. Cryst. Growth Des. (2010) 10.1021/cg100265d

[41]

Wu J.-Y. Cryst. Growth Des. (2009) 10.1021/cg8004163

[42]

Hu J. Bioorg. Med. Chem. Lett. (2010) 10.1016/j.bmcl.2010.06.079

[43]

Huang X. B. Polymer (2010) 10.1016/j.polymer.2010.05.001

[44]

Zheng L. F. Synlett (2010)

[45]

Hung H.-C. Eur. J. Org. Chem. (2090)

Cited By

57

Spin Crossover in Fe(II) and Co(II) Complexes with the Same Click-Derived Tripodal Ligand

David Schweinfurth, Serhiy Demeshko · 2014

Inorganic Chemistry

Synthesis and Characterization of Platinum(II) Complexes with a Diazenecarboxamide‐Appended Picolyl‐Triazole Ligand

Damijana Urankar, Andrej Pevec · 2011

European Journal of Inorganic Chemi...

Metrics

57

Citations

45

References

Details

Published: Oct 04, 2010
Vol/Issue: 10(11)
Pages: 4920-4927

Authors

D

Damijana Urankar

Faculty of Chemistry and Chemical Technology, University of Ljubljana, Aškerc̆eva 5, SI-1000 Ljubljana, Slovenia

A

Andrej Pevec

Faculty of Chemistry and Chemical Technology, University of Ljubljana, Aškerc̆eva 5, SI-1000 Ljubljana, Slovenia

I

Iztok Turel

Faculty of Chemistry and Chemical Technology, University of Ljubljana, Aškerc̆eva 5, SI-1000 Ljubljana, Slovenia

J

Janez Košmrlj

Faculty of Chemistry and Chemical Technology, University of Ljubljana, Aškerc̆eva 5, SI-1000 Ljubljana, Slovenia

Cite This Article

Damijana Urankar, Andrej Pevec, Iztok Turel, et al. (2010). Pyridyl Conjugated 1,2,3-Triazole is a Versatile Coordination Ability Ligand Enabling Supramolecular Associations. Crystal Growth & Design, 10(11), 4920-4927. https://doi.org/10.1021/cg100993k

Pyridyl Conjugated 1,2,3-Triazole is a Versatile Coordination Ability Ligand Enabling Supramolecular Associations

You May Also Like