2021
DOI: 10.1039/d1dt00373a
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Synthesis and crystal structures of nickel(ii) and palladium(ii) complexes with o-carboranyl amidine ligands

Abstract: A number of new nido-carboranyl amidines 10-R(CH2)nNHC(Et)=HN-7,8-C2B9H11 (n = 2, R = OH, OMe, NMe2; n = 3, R = OH) were synthesized by nucleophilic addition of amino alcohols and...

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Cited by 22 publications
(15 citation statements)
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“…When complexes Ir1 or Ir2 aggregate, the long alkyl chain introduced into the Ir1 and Ir2 will hinder phosphorescence quenching, which is a result of π-π stacking. Moreover, the introduction of fluorene groups would restrict the intramolecular rotation, 46,47 which will lead to an enhancement of the radiative process and a decrement of the non-radiative process.…”
Section: Dalton Transactions Papermentioning
confidence: 99%
“…When complexes Ir1 or Ir2 aggregate, the long alkyl chain introduced into the Ir1 and Ir2 will hinder phosphorescence quenching, which is a result of π-π stacking. Moreover, the introduction of fluorene groups would restrict the intramolecular rotation, 46,47 which will lead to an enhancement of the radiative process and a decrement of the non-radiative process.…”
Section: Dalton Transactions Papermentioning
confidence: 99%
“…19 Thus, the propionitrile addition to nido -carborane in the presence of mercury( ii ) chloride was used to obtain 10-amino- nido -carborane and its derivatives. 19 d ,20…”
Section: Resultsmentioning
confidence: 99%
“…Synthesis of boronated amidines by the reaction of nucleophilic addition of amines to alkylnitrilium derivatives was first described for arachno-decaborate [72] and closo-decaborate [40,41,[73][74][75][76] anions. Later, amidines on the base of nido-carborane [77][78][79] and the closo-dodecaborate anion [80] were synthesized. The reactions of [(8-RC≡N-3,3 -Co(1,2-C 2 B 9 H 10 )(1 ,2 -C 2 B 9 H 11 ] (R = Me, Ph) with n-butylamine and diethylamine resulting in the corresponding amidines were reported as well [49].…”
Section: Resultsmentioning
confidence: 99%
“…Although the formation of mixtures of the E and Z isomers for organic amidines is well known [82], the presence of E-and Z-isomers in solutions of boronated amidines prepared by addition of primary amines to nitrilium derivatives of polyhedral boron hydrides was reported only for the nido-decaborane [72] and nido-carborane [77,79] based amidines. This could be an indication that for the other boronated amidines only one isomer is present in solution, or that the interconversion between the E-and Z-isomers is fast on the NMR time scale.…”
Section: Nucleophilic Addition Of Primary Aminesmentioning
confidence: 99%