TY - JOUR
T1 - Synthesis and comparison of transition metal complexes of abnormal and normal tetrazolylidenes
T2 - A neglected ligand species
AU - Schaper, Lars Arne
AU - Wei, Xuhui
AU - Altmann, Philipp J.
AU - Öfele, Karl
AU - Pöthig, Alexander
AU - Drees, Markus
AU - Mink, János
AU - Herdtweck, Eberhardt
AU - Bechlars, Bettina
AU - Herrmann, Wolfgang A.
AU - Kühn, Fritz E.
PY - 2013/6/17
Y1 - 2013/6/17
N2 - To date, only few examples of tetrazolylidene carbenes coordinated to transition metal complexes have been described. A direct comparison of "normal" tetrazolylidenes (1,4-substitution pattern) and "abnormal" tetrazolylidenes (also referred to as "mesoionic carbenes"; 1,3-substitution pattern) has not been performed at all. In this work, we describe coordination of both ligand types to a row of transition metals. For example, the first examples of tetrazolylidene Mo, Ag, or Ir complexes have been isolated and fully characterized. The mesoionic tetrazolylidene Ag compound 2d is shown to be a viable carbene transfer reagent. By means of NMR, IR, and Raman spectroscopy, as well as X-ray crystallography and computational results, the pronounced differences between the two ligand substitution patterns are highlighted. It is shown that simply changing the position of a methyl group from N3 to N4 in the heterocycle can cause enormous differences in ligand characteristics.
AB - To date, only few examples of tetrazolylidene carbenes coordinated to transition metal complexes have been described. A direct comparison of "normal" tetrazolylidenes (1,4-substitution pattern) and "abnormal" tetrazolylidenes (also referred to as "mesoionic carbenes"; 1,3-substitution pattern) has not been performed at all. In this work, we describe coordination of both ligand types to a row of transition metals. For example, the first examples of tetrazolylidene Mo, Ag, or Ir complexes have been isolated and fully characterized. The mesoionic tetrazolylidene Ag compound 2d is shown to be a viable carbene transfer reagent. By means of NMR, IR, and Raman spectroscopy, as well as X-ray crystallography and computational results, the pronounced differences between the two ligand substitution patterns are highlighted. It is shown that simply changing the position of a methyl group from N3 to N4 in the heterocycle can cause enormous differences in ligand characteristics.
UR - http://www.scopus.com/inward/record.url?scp=84879232030&partnerID=8YFLogxK
U2 - 10.1021/ic4005449
DO - 10.1021/ic4005449
M3 - Article
C2 - 23706110
AN - SCOPUS:84879232030
SN - 0020-1669
VL - 52
SP - 7031
EP - 7044
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 12
ER -