In Memoriam

A Primer of Gold Chemistry 49
63. Icosahedral WAu 12: a predicted closed-shell species, stabilized by aurophilic attraction and relativity and
in accord with the 18-electron rule, P. Pyykkö and N. Runeberg, Angew. Chem. Int. Ed., 2002, 4.1., 2174.
64. Experimental observation and confirmation of icosahedral W@Au 12 and Mo@Au 12 molecules, X. Li, B.
Kiran, J. Li, H.-J. Zhai, and L.-S. Wang, Angew. Chem. Int. Ed., 2002, 4.1., 4786.
65. The relevance of shape and size of Au 55 clusters, G. Schmid, Chem. Soc. Rev., 2008, 3.7., 1909.
66. Structure of a thiol monolayer-protected old nanoparticle at 1.1 Å resolution, P. D. Jadzinsky, G. Calero,
C. A. Ackerson, D. A. Bushnell, and R. D. Kornberg, Science, 2007, 3.1.8., 430.
67. Crystal structure of the gold nanoparticle [N(C 8H 17) 4][Au 25(SCH 2CH 2Ph) 18], M. W. Heaven, A. Dass,
P. S. White, K. M. Holt, and R. W. Murray, J. Am. Chem. Soc., 2008, 1.3.0., 3754.
68. Correlating the crystal structure of a thiol-protected Au cluster and optical properties, M. Zhu, C. M.
Aikens, F. J. Hollander, G. C. Schatz, and R. Jin, J. Am. Chem. Soc., 2008, 1.3.0., 5883.
69. On the structure of thiolate-protected Au, J. Akola, M. Walter, R. L. Whetten, H. Häkkinen, and H. Grönbeck,
J. Am. Chem. Soc., 2008, 1.3.0., 3756.
70. Conversion of anionic [Au 25(SCH 2CH 2Ph) 18] cluster to charge neutral cluster via air oxidation, M. Zhu,
W. T. Eckenhoff, T. Pintauer, and R. Jin, J. Phys. Chem. C, 2008, 1.1.2., 14221.
71. Chalcogenide centred gold complexes, M. C. Gimeno and A. Laguna, Chem. Soc. Rev., 2008, 3.7., 1952.
72. An organometallic approach to gold nanoparticles: synthesis and X-ray structure of CO-protected
Au 21Fe 10, Au 22Fe 12, Au 28Fe 14 and Au 34Fe 14 clusters, C. Femoni, M. C. Iapalucci, G. Longoni, C. Tiozzo,
and S. Zacchini, Angew. Chem. Int. Ed., 2008, 4.7., 6666.
73. Gold-based therapeutic agents, C. F. Shaw III, Chem. Rev., 1999, 9.9., 2589.
74. Gold(III) compounds as anticancer drugs, C. Gabbiani, A. Casini, and Luigi Messori, Gold Bulletin,
2007, 4.0., 73.
75. Targeting the mitochondrial cell death pathway with gold compounds, P. J. Barnard and S. J. Berners-
Price, Coord. Chem. Rev. 2007, 2.5.1., 188.
76. Gold catalysis, A. S. K. Hashmi and G. J. Hutchings, Angew. Chem. Int. Ed., 2006, 4.5., 7896.
77. Gold-catalyzed organic transformations, Z. Li, C. Brouwer, and C. He, Chem. Rev., 2008, 1.0.8., 3239.
78. Alternative synthetic methods through new developments in catalysis by gold, A. Arcadi, Chem. Rev.,
2008, 1.0.8., 3266
79. Gold-catalyzed cycloisomerizations of enynes: a mechanistic perspective, E. Jiménez-Núñez and A. M.
Echavarren, Chem. Rev., 2008, 1.0.8., 3326.
80. Ligand effects in homogeneous Au catalysis, D. J. Gorin, B. D. Sherry, and F. D. Toste, Chem. Rev., 2008,
1.0.8., 3351.
81. Coinage metal catalyzed C−H bond functionalization of hydrocarbons, M. M. Díaz-Requejo and P. J.
Pérez, Chem. Rev., 2008, 1.0.8., 3379.
82. Coinage metal-assisted synthesis of heterocycles, N. T. Patil and Y. Yamamoto, Chem. Rev., 2008, 1.0.8.,
3395.