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022 _a09743626
040 _aMSU
_bEnglish
_cMSU
_erda
050 0 0 _aQD31 JOU
100 1 _aNaktode, K.
_eauthor
245 1 0 _aSyntheses and structures of dimeric sodium and potassium complexes of 2,6-diisopropyl-anilidophosphine borane ligand /
_ccreated by K. Naktode, Jayeeta Bhattacharjee, Anirban Chakrabarti and T. Panda
264 1 _aBangalore :
_bSpringer,
_c2015.
336 _2rdacontent
_atext
_btxt
337 _2rdamedia
_aunmediated
_bn
338 _2rdacarrier
_avolume
_bnc
440 _aJournal of chemical sciences
_vVolume 127, number 2,
520 3 _aWe report here the syntheses and structural studies of dimeric sodium and potassium complexes of composition [Na(THF)2{Ph2P(BH3)N(2,6-iPr2C6H6)}]2 (2) and [K(THF)2{Ph2P(BH3)N(2,6-iPr2C6H6)}]2 (3). The sodium complex 2 was readily prepared by the reaction of sodium bis(trimethylsilyl)amide with 2,6-diisopropylanilidophosphine-borane ligand [2,6-iPr2C6H3NHP(BH3)Ph2] (1-H) at ambient temperature. The potassium complex 3 was prepared by two synthetic routes: in the first method, the ligand 1-H was made to react with potassium hydride at room temperature to afford the corresponding potassium complex. The potassium bis(trimethylsilyl)amides were made to react with protic ligand 1-H in the second method to eliminate the volatile bis(trimethyl)silyl amine. Solid-state structures of both the new complexes were established by single crystal X-ray diffraction analysis. In the molecular structures of complexes 2, the sodium metal is coordinated by the anilido nitrogen (η 1) and borane group (η 1) attached to the phosphorus atom of ligand 1. In contrast, for compound 2, ligand 1 displays η 6 π-arene interaction from 2,6-diisopopylphenyl ring with potassium atom along with η 3 interaction of BH3 group due to larger ionic radius of potassium ion.
650 _aSodium
_vPotassium
_xπ-arene interaction
700 1 _aBhattacharjee, Jayeeta
_eco author
700 1 _aChakrabarti, Anirban
_eco author
700 1 _aPanda, T.
_eco author
856 _uhttps://doi.org/10.1007/s12039-015-0782-5
942 _2lcc
_cJA
999 _c169256
_d169256