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Macrocyclic ligand design. Effect of donor-set and ringsize variation on silver(I)/lead(II) discrimination within an extended series of dibenzo substituted rings

journal contribution
posted on 2023-04-03, 17:08 authored by Kenneth R Adam, Darren S Baldwin, Paul A Duckworth, Leonard F Lindoy, Mary McPartlin, Alan Bashall, Harold R Powell, Peter A Tasker
Murray-Darling Freshwater Research Centre

MDFRC item.

The effect of systematic variation of the donor-atom set within dibenzo-substituted, 17- to 20-membered macrocycles on their ability to discriminate between silver(I) and lead(II) has been investigated. The log K values for the respective complexes. determined potentiometrically in 95% methanol (l = 0.1 mol dm(-3), NEt(4)ClO(4)), show that successive replacement of either nitrogen or oxygen heteroatoms by thioether donors leads to increasing affinity for silver(I) relative to lead(II), as does the incorporation of an 'aliphatic' NON or NSN donor sequence in the structure. For the 17-membered system incorporating a S2N2S-donor set, exceptional discrimination (of the order of 10(9)) was observed. The characterisation of selected complexes has included the crystal structure of the sliver perchlorate complex of the 17-membered ON2S2 macrocycle (L(17)). The silver ion in [AgL(17)]ClO4 has a very distorted trigonal-bipyramidal geometry with all metal to donor bond lengths appearing normal. The complex crystallises in the monoclinic space group P2(1)/n with lattice parameters a = 19.410(4), b = 9.602(2), c = 12.747(3) Angstrom, beta = 103.67(2)degrees and Z = 4.

History

Publication Date

1995-07-01

Journal

Journal of the Chemical Society Dalton transactions.

Volume

7

Pagination

1127-1131

Publisher

UK: RSC Publishing.

Data source

arrow migration 2023-03-15 20:45. Ref: f1b71f. IDs:['http://hdl.handle.net/1959.9/492288', 'latrobe:32948']

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