TY - JOUR
T1 - X-ray crystallographic studies and dynamic 1H NMR spectroscopic studies of the novel sodium aza-allyl monomer [PhC(H)NC(H)Ph]Na · PMDETA
T2 - A discrete contact ion-pair structure held together by a short NNa bond, and showing close (ortho-Ph)CH ··· Na contacts in both solid state and solution
AU - Andrews, Philip C.
AU - Mulvey, Robert E.
AU - Clegg, William
AU - Reed, David
PY - 1990/4/17
Y1 - 1990/4/17
N2 - [PhC(H)NC(H)Ph]Na · PMDETA (1) (PMDETA = (Me2NCH2CH2)2NMe), exhibits a contact ion-pair arrangement in the crystal, with the complexed metal cation bound to the nitrogen centre of the aza-allyl {A figure is presented} fragment (NNa bond length, 2.384(2) Å). Further close contacts exist between the sodium and one ortho-C from each phenyl ring (distances 3.133(4) and 3.166(4) Å). Variable-temperature 1H NMR spectroscopic studies indicate that 1 adopts a remarkably similar structure in tetrahydrofuran-d8 solution. Thus, at -50°C the restricted rotation about each C(ipso)C(benzylic) bond results in the appearance of two distinct resonances each for both the ortho- and meta-H's. From their coalescence temperatures the energy barrier to rotation has been estimated (12.8 kcal mol-1). Evidence that this rigid solution conformation mimics the crystal structure in having short ortho-CH ··· Na distances comes from the exceptionally large chemical shift difference (1.05 ppm) associated with the dual ortho-H signals.
AB - [PhC(H)NC(H)Ph]Na · PMDETA (1) (PMDETA = (Me2NCH2CH2)2NMe), exhibits a contact ion-pair arrangement in the crystal, with the complexed metal cation bound to the nitrogen centre of the aza-allyl {A figure is presented} fragment (NNa bond length, 2.384(2) Å). Further close contacts exist between the sodium and one ortho-C from each phenyl ring (distances 3.133(4) and 3.166(4) Å). Variable-temperature 1H NMR spectroscopic studies indicate that 1 adopts a remarkably similar structure in tetrahydrofuran-d8 solution. Thus, at -50°C the restricted rotation about each C(ipso)C(benzylic) bond results in the appearance of two distinct resonances each for both the ortho- and meta-H's. From their coalescence temperatures the energy barrier to rotation has been estimated (12.8 kcal mol-1). Evidence that this rigid solution conformation mimics the crystal structure in having short ortho-CH ··· Na distances comes from the exceptionally large chemical shift difference (1.05 ppm) associated with the dual ortho-H signals.
UR - http://www.scopus.com/inward/record.url?scp=0000599879&partnerID=8YFLogxK
U2 - 10.1016/0022-328X(90)80001-G
DO - 10.1016/0022-328X(90)80001-G
M3 - Article
AN - SCOPUS:0000599879
SN - 0022-328X
VL - 386
SP - 287
EP - 297
JO - Journal of Organometallic Chemistry
JF - Journal of Organometallic Chemistry
IS - 3
ER -