Lithium N,N'-bis(trimethylsilyl)heterocyclic amidinate complexes with 3- and 4-pyridyl and 3-furyl carbon substituents were prepared by addition of the corresponding nitriles to LiN(SiMe3)(2) (LiNTMS2) solution, In the presence of NA, IV, N' tetramethylethylene diamine (TIVIEDA), both pyndyl amidinates crystallize as coordination polymers with an amidinate-Li-pyridyl backbone. The 4-pyridyl derivative (7) creates a linear polymerwith amidinate-Li-TMEDA units as sidechains, whereas the 3-pyridyl polymer (6) has a two-dimensional (2D) network structure in which TMEDA serves as across-linker. Solvation of the reaction mixture of 3-furonitrile and LiNTMS2 with TMEDA affords the monomeric 3furyl amidinate Li TMEDA complex (3). Crystals of the Li2O complex {[3-furyl-C-(NTMS)(2)Li}(4)center dot Li2O}center dot C7H8 (4) are obtained from toluene by partial hydrolysis of the unsolvated 3-furyl arniclinate (2). Degradation of the polymer (7) to monomeric units can be achieved by solvation in toluene or by reaction with TMS2NLi.TMEDA that affords crystals of the complex {NTMS2Li center dot[4-C5H4N-C(NTMS)(2)Li center dot TMEDA]}2 center dot(NTMS2Li center dot TMEDA) (8). The formation of these aggregates can be rationalized by directed substitution of TMEDA with pyridyl moieties and by the laddering principle.