Synthesis of [{AgO₂CCH₂OMe(PPh₃)}_n] and theoretical study of its use in focused electron beam induced deposition

• Jelena Tamuliene,
• Julian Noll,
• Peter Frenzel,
• Tobias Rüffer,
• Alexander Jakob,
• Bernhard Walfort and
• Heinrich Lang

Beilstein J. Nanotechnol. 2017, 8, 2615–2624, doi:10.3762/bjnano.8.262

• ; υasym = 1615 cm−1, υsym = 1423 cm−1), confirming that in the respective carboxylate complexes the organic ligand is µ-bridging the silver atoms [13]. This bonding motif was confirmed by single crystal X-ray diffraction analysis of 2 (Figure 1). In addition, EI and high-resolution ESI–TOF mass

Rigid multipodal platforms for metal surfaces

• Michal Valášek,
• Marcin Lindner and
• Marcel Mayor

Beilstein J. Nanotechnol. 2016, 7, 374–405, doi:10.3762/bjnano.7.34

Synthesis, characterization, monolayer assembly and 2D lanthanide coordination of a linear terphenyl-di(propiolonitrile) linker on Ag(111)

• Zhi Chen,
• Svetlana Klyatskaya,
• José I. Urgel,
• David Écija,
• Olaf Fuhr,
• Willi Auwärter,
• Johannes V. Barth and
• Mario Ruben

Beilstein J. Nanotechnol. 2015, 6, 327–335, doi:10.3762/bjnano.6.31

• and metal coordination at interfaces. The structure of the organic linker 2 was confirmed by single crystal X-ray diffraction analysis (XRD). On the densely packed Ag(111) surface, the terphenyl-4,4"-di(propiolonitrile) linkers self-assemble in a regular, molecular chevron arrangement exhibiting a

• ; molecular self-assembly; organic monolayers; single crystal X-ray diffraction analysis; UHV-STM; Introduction The drive towards miniaturization of modern electronics has led to a growing interest in the development of memory units that can satisfy the ever-growing demand for information storage. In this

• single crystal X-ray diffraction analysis (XRD) along with other standard techniques (Supporting Information File 1). The results of the surface-confined, molecular self-assembly and the lanthanide coordination reaction were analysed by using low-temperature scanning tunnelling microscopy (STM). The STM