Tunable N-substitution in zwitterionic benzoquinonemonoimine derivatives: Metal coordination, tandemlike synthesis of zwitterionic metal complexes, and supramolecular structures

Full details on a very efficient transamination reaction for the synthesis of zwitterionic N,N'-dialkyl-2-amino-5-alcoholate-1,4-benzoquinone-monoiminium derivatives [C6H2-(- NHR)(2)(- O)(2)] 5-16 are reported. The molecular structures of zwitterions 5 (R = CH3) in 5 center dot H2O, 13 (R = CH2CH2OMe) 15 (R = CH2CH2NMe2), and of the parent, unsubstituted system [C6H2(- NH2)(2)(- O)(2)] 4 in 4 center dot H2O have been established by single-crystal Xray diffraction. This one-Pot preparation can be carried out in water, MeOH, or EtOH and allows access to new zwitterions with N-substituents bearing functionalities such as -OMe (13), -OH (9-12), -(NRR2)-R-1 with R-1 = or not equal R-2 (14-16) or an alkene (8), leading to a rich coordination chemistry and allowing fine-tuning of the supramolecular arrangements in the solid state. As previously described for 15, which reacted with Zn(acac)(2) to afford the octahedral Zn-II complex [Zn{C6H2(=NCH2CH2NMe2)O(=O)-(NHCH2CH2NMe2)}(2)] (20), ligands 13 and 16 with coordinating arms afforded with Zn(acac)(2) the 2:1 adducts [Zn{C6H2(=NCH2CH2X)O(=O)(NHCH2CH2NX)}(2)] 19 (X=OMe) and 21 (X=NHEt), with N2O4, and N4O2 donor sets around the octahedral Zn-II center, respectively. Furthermore, zwitterions 15 and 16 reacted with ZnCl2 to give the stable, crystallographically characterized Zn-II zwitterionic complexes [ZnCl2{C6H2(=(NCH2CH2NRR2)-R-1)O(=O)- ((NHCH2CH2NHRR2)-R-1)}] 22 (R-1 = R-2 = Me) and 23 (R-1 = Et, R-2 = H) by means of an unprecedented, tandemlike synthesis in which 1) the two pendant amino groups of the organic benzoquinonemonoimine zwitterionic precursor favor metal coordination and proton transfer and 2) the saturated linker prevents pi-conjugation between the charges. The nature of the structural arrangements in the solid state for both inorganic (20, 22 23) and organic (5, 9, 13, and 15) molecules is determined by subtle variations in the nature of the N-substituent on the zwitterion precursor.