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Search for "organometallic synthesis" in Full Text gives 2 result(s) in Beilstein Journal of Nanotechnology.

Electron-induced ligand loss from iron tetracarbonyl methyl acrylate

Beilstein J. Nanotechnol. 2024, 15, 797–807, doi:10.3762/bjnano.15.66

probable reasons are its availability (it is a common precursor for iron-containing compounds in organometallic synthesis), ease of handling (it is a volatile liquid at standard conditions), and relatively simple structure, which allows for advanced theoretical description. The ligand loss from Fe(CO)5 in

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Published 03 Jul 2024

Beilstein J. Nanotechnol. 2010, 1, 108–118, doi:10.3762/bjnano.1.13

corresponding to the large hyperfine fields with large isomer shifts are indeed characteristic of surface atoms. Keywords: iron nanoparticles; magnetic properties; organometallic synthesis; size effects; structure; Introduction Progress in both experimental techniques and theoretical calculations over the

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Published 03 Dec 2010

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aromatic	the word “aromatic”
aromatic aldehyde	the word “aromatic” OR “aldehyde”
+aromatic +aldehyde	both words “aromatic” AND “aldehyde”
+aromatic -aldehyde	the word “aromatic” but NOT “aldehyde”
“aromatic aldehyde”	the exact phrase “aromatic aldehyde”
benz*	words which begin with “benz”, such as “benzene” or “benzyl”
benz*yl	words that begin with “benz” and end with “yl”, such as “benzyl” or “benzoyl”
benzyl~	words that are close to the word “benzyl”, such as “benzoyl” (i.e., fuzzy search)