“…. HB interactions preserve in the benzene solution (2380 cm´1) [82]. As it was revealed by 11 B NMR spectroscopy, the same is true for the solution of Ag[CB 11 H 12 ] in dichloromethane [83].…”
Section: Silver Complexes With the 1-carba-closo-decaborate Anion [1-supporting
ianion, the structure of which contains two four-coordinated boron atoms, to very weak M . . . H interactions with the hydride atoms in the case of bulky [3,3 1 -Co(1,2-C 2 B 9 H 11 ) 2 ]´monoanion.
“…. HB interactions preserve in the benzene solution (2380 cm´1) [82]. As it was revealed by 11 B NMR spectroscopy, the same is true for the solution of Ag[CB 11 H 12 ] in dichloromethane [83].…”
Section: Silver Complexes With the 1-carba-closo-decaborate Anion [1-supporting
ianion, the structure of which contains two four-coordinated boron atoms, to very weak M . . . H interactions with the hydride atoms in the case of bulky [3,3 1 -Co(1,2-C 2 B 9 H 11 ) 2 ]´monoanion.
“…2387 cm -1 ). Similar shifts of ν(BH) were previously reported for related silver salts and complexes of carba-closododecaborate anions [1,18,20,22] and for polymeric {Ag 2 (12-C≡C-closo-1-CB 11 H 11 )} n . [5] The other BH-stretching bands in the IR spectrum of [Ag1] are shifted to slightly higher wavenumbers, compared with [EMIm]1 ( Figure 5).…”
Section: Vibrational Spectroscopysupporting
confidence: 85%
“…[18] The benzene ring is slightly distorted from an ideal geometry in the experimental and the calculated structures. The CC bond that interacts with silver(I) is longer than the other five bonds, which have alternating lengths (Table 1).…”
“…The (34). Quantitative C 6 F 5 transfer was complete after 12 h to give 34 as the unique reaction product, isolated as a crystalline solid.…”
Section: Catalytic Activity and Deactivation Of Cationic Compoundsmentioning
confidence: 99%
“…6. The pseudo-tetrahedral geometry about Ti and Zr in 29 and 30 is defined by the centroid of the cyclopentadienyl ring and the two N-donors of the appended (dimethylsilyl)amido arms, with the remaining coordination site occupied by the meta-C atom of the benzylborate phenyl ring indicating an interaction of its pp orbital with the empty hybrid metal orbital [34][35][36].…”
We present in this account the synthesis and recent developments of a new class of group 4 metal complexes with the tridentate di(silylamido)cyclopentadienyl ligand. These doubly silyl-bridged group 4 metal amido chelates are receiving increasing interest as they are efficient catalysts for ethene polymerization when activated with MAO despite generating 14-electron d 0 cationic species free of the alkyl group required for the first insertion reaction in the polymerization process.
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