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Fullerenium salts: a new class of C60-based compounds.

Journal of the American Chemical Society

Riccò M, Pontiroli D, Mazzani M, Gianferrari F, Pagliari M, Goffredi A, Brunelli M, Zandomeneghi G, Meier BH, Shiroka T.
PMID: 20102192
J Am Chem Soc. 2010 Feb 17;132(6):2064-8. doi: 10.1021/ja909614x.

We report here on the preparation and characterization of a fullerenium salt in the solid state, where the fullerene is in the 2+ oxidized state. To succeed in this long-standing challenge, we exploit the oxidizing power of one of...

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Riccò M, Pontiroli D, Mazzani M, et al. Fullerenium salts: a new class of C60-based compounds. J Am Chem Soc. 2010;132(6):2064-8doi: 10.1021/ja909614x.
Riccò, M., Pontiroli, D., Mazzani, M., Gianferrari, F., Pagliari, M., Goffredi, A., Brunelli, M., Zandomeneghi, G., Meier, B. H., & Shiroka, T. (2010). Fullerenium salts: a new class of C60-based compounds. Journal of the American Chemical Society, 132(6), 2064-8. https://doi.org/10.1021/ja909614x
Riccò, Mauro, et al. "Fullerenium salts: a new class of C60-based compounds." Journal of the American Chemical Society vol. 132,6 (2010): 2064-8. doi: https://doi.org/10.1021/ja909614x
Riccò M, Pontiroli D, Mazzani M, Gianferrari F, Pagliari M, Goffredi A, Brunelli M, Zandomeneghi G, Meier BH, Shiroka T. Fullerenium salts: a new class of C60-based compounds. J Am Chem Soc. 2010 Feb 17;132(6):2064-8. doi: 10.1021/ja909614x. PMID: 20102192.
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A mechanical model for the half-of-the-sites reactivity of oligomeric enzymes.

Biophysical chemistry

Luisi PL, Zandomeneghi M.
PMID: 23260424
Biophys Chem. 1974 May;1(5):358-66. doi: 10.1016/0301-4622(74)85005-2.

We developed a model which is able to provide a rationalization of the half-of-the-sites reactivity of oligomeric enzymes. According to this model, a dimeric enzyme is considered as a system of two coupled oscilators, which are able to transmit...

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Luisi PL, Zandomeneghi M. A mechanical model for the half-of-the-sites reactivity of oligomeric enzymes. Biophys Chem. 1974;1(5):358-66doi: 10.1016/0301-4622(74)85005-2.
Luisi, P. L., & Zandomeneghi, M. (1974). A mechanical model for the half-of-the-sites reactivity of oligomeric enzymes. Biophysical chemistry, 1(5), 358-66. https://doi.org/10.1016/0301-4622(74)85005-2
Luisi, P L, and Zandomeneghi, M. "A mechanical model for the half-of-the-sites reactivity of oligomeric enzymes." Biophysical chemistry vol. 1,5 (1974): 358-66. doi: https://doi.org/10.1016/0301-4622(74)85005-2
Luisi PL, Zandomeneghi M. A mechanical model for the half-of-the-sites reactivity of oligomeric enzymes. Biophys Chem. 1974 May;1(5):358-66. doi: 10.1016/0301-4622(74)85005-2. PMID: 23260424.
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Manipulation of the director in bicellar mesophases by sample spinning: a new tool for NMR spectroscopy.

Journal of the American Chemical Society

Zandomeneghi G, Tomaselli M, van Beek JD, Meier BH.
PMID: 11456624
J Am Chem Soc. 2001 Feb 07;123(5):910-3. doi: 10.1021/ja0019326.

It is shown that bicellar nematic liquid-crystalline phases can be oriented with the director (the normal to the bicellar plane) at an arbitrary angle to the applied magnetic field by sample rotation around one axis (variable-angle sample spinning) or...

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Zandomeneghi G, Tomaselli M, van Beek JD, et al. Manipulation of the director in bicellar mesophases by sample spinning: a new tool for NMR spectroscopy. J Am Chem Soc. 2001;123(5):910-3doi: 10.1021/ja0019326.
Zandomeneghi, G., Tomaselli, M., van Beek, J. D., & Meier, B. H. (2001). Manipulation of the director in bicellar mesophases by sample spinning: a new tool for NMR spectroscopy. Journal of the American Chemical Society, 123(5), 910-3. https://doi.org/10.1021/ja0019326
Zandomeneghi, G, et al. "Manipulation of the director in bicellar mesophases by sample spinning: a new tool for NMR spectroscopy." Journal of the American Chemical Society vol. 123,5 (2001): 910-3. doi: https://doi.org/10.1021/ja0019326
Zandomeneghi G, Tomaselli M, van Beek JD, Meier BH. Manipulation of the director in bicellar mesophases by sample spinning: a new tool for NMR spectroscopy. J Am Chem Soc. 2001 Feb 07;123(5):910-3. doi: 10.1021/ja0019326. PMID: 11456624.
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Database of multi-parametric geophysical data from the TOMO-DEC experiment on Deception Island, Antarctica.

Scientific data

Ibáñez JM, Díaz-Moreno A, Prudencio J, Zandomeneghi D, Wilcock W, Barclay A, Almendros J, Benítez C, García-Yeguas A, Alguacil G.
PMID: 28895947
Sci Data. 2017 Sep 12;4:170128. doi: 10.1038/sdata.2017.128.

Deception Island volcano (Antarctica) is one of the most closely monitored and studied volcanoes on the region. In January 2005, a multi-parametric international experiment was conducted that encompassed both Deception Island and its surrounding waters. We performed this experiment...

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Ibáñez JM, Díaz-Moreno A, Prudencio J, et al. Database of multi-parametric geophysical data from the TOMO-DEC experiment on Deception Island, Antarctica. Sci Data. 2017;4:170128doi: 10.1038/sdata.2017.128.
Ibáñez, J. M., Díaz-Moreno, A., Prudencio, J., Zandomeneghi, D., Wilcock, W., Barclay, A., Almendros, J., Benítez, C., García-Yeguas, A., & Alguacil, G. (2017). Database of multi-parametric geophysical data from the TOMO-DEC experiment on Deception Island, Antarctica. Scientific data, 4170128. https://doi.org/10.1038/sdata.2017.128
Ibáñez, Jesús M, et al. "Database of multi-parametric geophysical data from the TOMO-DEC experiment on Deception Island, Antarctica." Scientific data vol. 4 (2017): 170128. doi: https://doi.org/10.1038/sdata.2017.128
Ibáñez JM, Díaz-Moreno A, Prudencio J, Zandomeneghi D, Wilcock W, Barclay A, Almendros J, Benítez C, García-Yeguas A, Alguacil G. Database of multi-parametric geophysical data from the TOMO-DEC experiment on Deception Island, Antarctica. Sci Data. 2017 Sep 12;4:170128. doi: 10.1038/sdata.2017.128. PMID: 28895947; PMCID: PMC5595047.
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Determination of the photochemical efficiency of o-quinodimethane ring closure in room-temperature solutions by using time-delayed, two-color photolysis technique.

The Journal of organic chemistry

Ouchi A, Sakuragi M, Kitahara H, Zandomeneghi M.
PMID: 10789446
J Org Chem. 2000 Apr 21;65(8):2350-7. doi: 10.1021/jo991518s.

Photochemical efficiency of o-quinodimethane (3) ring closure at room temperature was determined by using a time-delayed, two-color photolysis technique. o-Quinodimethane (3) was generated by the photolysis of 1,2-bis[(phenylseleno)methyl]benzene (1) by a KrF (248 nm) laser pulse and thus-generated 3...

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Ouchi A, Sakuragi M, Kitahara H, et al. Determination of the photochemical efficiency of o-quinodimethane ring closure in room-temperature solutions by using time-delayed, two-color photolysis technique. J Org Chem. 2000;65(8):2350-7doi: 10.1021/jo991518s.
Ouchi, A., Sakuragi, M., Kitahara, H., & Zandomeneghi, M. (2000). Determination of the photochemical efficiency of o-quinodimethane ring closure in room-temperature solutions by using time-delayed, two-color photolysis technique. The Journal of organic chemistry, 65(8), 2350-7. https://doi.org/10.1021/jo991518s
Ouchi, et al. "Determination of the photochemical efficiency of o-quinodimethane ring closure in room-temperature solutions by using time-delayed, two-color photolysis technique." The Journal of organic chemistry vol. 65,8 (2000): 2350-7. doi: https://doi.org/10.1021/jo991518s
Ouchi A, Sakuragi M, Kitahara H, Zandomeneghi M. Determination of the photochemical efficiency of o-quinodimethane ring closure in room-temperature solutions by using time-delayed, two-color photolysis technique. J Org Chem. 2000 Apr 21;65(8):2350-7. doi: 10.1021/jo991518s. PMID: 10789446.
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The crystal structure of D-ribose--at last!.

Angewandte Chemie (International ed. in English)

Sisak D, McCusker LB, Zandomeneghi G, Meier BH, Bläser D, Boese R, Schweizer WB, Gilmour R, Dunitz JD.
PMID: 20468021
Angew Chem Int Ed Engl. 2010 Jun 14;49(26):4503-5. doi: 10.1002/anie.201001266.

No abstract available.

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Sisak D, McCusker LB, Zandomeneghi G, et al. The crystal structure of D-ribose--at last!. Angew Chem Int Ed Engl. 2010;49(26):4503-5doi: 10.1002/anie.201001266.
Sisak, D., McCusker, L. B., Zandomeneghi, G., Meier, B. H., Bläser, D., Boese, R., Schweizer, W. B., Gilmour, R., & Dunitz, J. D. (2010). The crystal structure of D-ribose--at last!. Angewandte Chemie (International ed. in English), 49(26), 4503-5. https://doi.org/10.1002/anie.201001266
Sisak, Dubravka, et al. "The crystal structure of D-ribose--at last!." Angewandte Chemie (International ed. in English) vol. 49,26 (2010): 4503-5. doi: https://doi.org/10.1002/anie.201001266
Sisak D, McCusker LB, Zandomeneghi G, Meier BH, Bläser D, Boese R, Schweizer WB, Gilmour R, Dunitz JD. The crystal structure of D-ribose--at last!. Angew Chem Int Ed Engl. 2010 Jun 14;49(26):4503-5. doi: 10.1002/anie.201001266. PMID: 20468021.
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Showing 1 to 6 of 6 entries