Syntheses of the First Coordination Compounds of the New Strong Molecular Electron Donor and Double Proton Sponge 1,4,5,8‐Tetrakis(tetramethylguanidino)naphthalene

Abstract

Abstract Herein we report on the synthesis and properties of a new electron donor featuring an aromatic system to which four guanidino groups are attached, namely, 1,4,5,8‐tetrakis(tetramethylguanidino)naphthalene (ttmgn). The molecule is a double proton sponge with an asymmetric N–H ··· N bridge being formed in the protonated form. Oxidation is followed electrochemically, and two oxidation waves at E 1/2 (CH 3 CN) = –0.25 and +0.50 V vs. SCE are observed. Chemical oxidation with I 2 yields ttmgn(I 3 ) 2 , in which the I 3 – units interact with the ttmgn 2+ cations through I ··· C contacts. Reaction with an excess amount of Br 2 leads to removal of four electrons from the aromatic system and formation of the salt (ttmgn)Br 4 with a chair‐type conformation of the C 10 core. The binuclear Al alkyl complex [(ttmgn)(AlMe 2 ) 2 ][BPh 4 ] 2 can be prepared by reaction between the diprotonated ttmgn molecule and AlMe 3 and serves as a benchmark system for the understanding of dynamic effects. Magnetic superexchange through the ligand unit is studied for the binuclear Co II complex [(ttmgn)(CoCl 2 ) 2 ]. SQUID measurements show an extremely weak antiferromagnetic coupling. The coupling might be affected by the unusual geometry of the coordination compounds of ttmgn, in which the metal ions are significantly displaced from the plane defined by the aromatic ring of the ttmgn ligand. We also report the analogous Co complex of ttmgb [ttmgb = 1,2,4,5‐tetrakis(tetramethylguanidino)benzene], namely, [(ttmgb)(CoCl 2 ) 2 ], in which the bonding situation is quite different.