5 research outputs found
The amino alcohol MeN(CH2CMe2OH)2
The crystal structure, including a graph-set analysis, of 1-[(2-hydroxy-2-methylpropyl)methylamino]-2-methylpropan-2-ol, C9H21NO2, is reported. The structure is characterized by unsymmetrical intra- and intermolecular O—H...O hydrogen bridges, giving rise to the formation of an infinite polymer consisting of eight-membered rings arranged in zigzag chains running along the a axis
The sodium chloride complex catena-poly[[{μ3-2-[bis(2-hydroxyethyl)amino]ethan-1-ol}sodium] chloride], N(CH2CH2OH)3·NaCl
The reaction of sodium chloride with 2-[bis(2-hydroxyethyl)amino]ethan-1-ol results in the formation of the title salt {[Na{N(CH2CH2OH)3}]Cl}n. The polymeric structure is characterized by a sodium cation coordinated by one nitrogen and five oxygen atoms in a distorted octahedral environment. The resulting one-dimensional {—O—Na—O—Na—O}— coordination polymer extends parallel to [010] and is connected through the chloride counter-anion via O—H...Cl hydrogen bonding, giving rise to a two-dimensional supramolecular structure parallel to (001)
The sodium chloride complex catena-poly[[{μ3-2-[bis(2-hydroxyethyl)amino]ethan-1-ol}sodium] chloride], N(CH2CH2OH)3·NaCl
The reaction of sodium chloride with 2-[bisÂ(2-hyÂdroxyÂethÂyl)amino]Âethan-1-ol results in the formation of the title salt {[Na{N(CH2CH2OH)3}]Cl}n. The polymeric structure is characterized by a sodium cation coordinated by one nitroÂgen and five oxygen atoms in a distorted octaÂhedral environment. The resulting one-dimensional {—O—Na—O—Na—O}— coordination polymer extends parallel to [010] and is connected through the chloride counter-anion via O—H...Cl hydrogen bonding, giving rise to a two-dimensional supraÂmolecular structure parallel to (001)
Simplicity Meets Beauty. Trapping Molecular Dimethyltin Oxide in the Novel Organotinoxo Cluster [MeN(CH<sub>2</sub>CH<sub>2</sub>O)<sub>2</sub>SnMe<sub>2</sub>·Me<sub>2</sub>SnO]<sub>3</sub>
The
syntheses are reported of the 1,1,5-trimethyl-2,8-dioxa-5-aza-1-stannabicyclo[3.3.0]Âoctane
MeNÂ(CH<sub>2</sub>CH<sub>2</sub>O)<sub>2</sub>SnMe<sub>2</sub> (<b>1</b>), its monosodium aminoalcoholate adduct [MeNÂ(CH<sub>2</sub>CH<sub>2</sub>O)<sub>2</sub>SnMe<sub>2</sub>·MeNÂ(CH<sub>2</sub>CH<sub>2</sub>ONa)Â(CH<sub>2</sub>CH<sub>2</sub>OH)]<sub>2</sub> (<b>2</b>), and the hexanuclear organotin oxo cluster [MeNÂ(CH<sub>2</sub>CH<sub>2</sub>O)<sub>2</sub>SnMe<sub>2</sub>·Me<sub>2</sub>SnO]<sub>3</sub> (<b>3</b>). The compounds were characterized
by <sup>1</sup>H, <sup>13</sup>C, and <sup>119</sup>Sn NMR spectroscopy,
electrospray ionization mass spectrometry, and single-crystal X-ray
diffraction analysis. In the solid state, compound <b>1</b> is
a tetramer that is brought about by intermolecular O→Sn interactions.
In solution, however, it shows a monomer ⇌ dimer equilibrium
that is fast on the <sup>1</sup>H, <sup>13</sup>C, and <sup>119</sup>Sn NMR time scales at room temperature. All compounds show intramolecular
N→Sn interactions at Sn–N distances ranging between
2.378(3) Å (<b>2</b>) and 3.026(3) Å (<b>3</b>·0.25H<sub>2</sub>O). Compound <b>3</b> can formally be
regarded as a molecular dimethyltin oxide being trapped by head-to-tail
complexation with a stannabicyclooctane. In solution, it slowly falls
apart into <b>1</b> and Me<sub>2</sub>SnO
Simplicity Meets Beauty. Trapping Molecular Dimethyltin Oxide in the Novel Organotinoxo Cluster [MeN(CH<sub>2</sub>CH<sub>2</sub>O)<sub>2</sub>SnMe<sub>2</sub>·Me<sub>2</sub>SnO]<sub>3</sub>
The
syntheses are reported of the 1,1,5-trimethyl-2,8-dioxa-5-aza-1-stannabicyclo[3.3.0]Âoctane
MeNÂ(CH<sub>2</sub>CH<sub>2</sub>O)<sub>2</sub>SnMe<sub>2</sub> (<b>1</b>), its monosodium aminoalcoholate adduct [MeNÂ(CH<sub>2</sub>CH<sub>2</sub>O)<sub>2</sub>SnMe<sub>2</sub>·MeNÂ(CH<sub>2</sub>CH<sub>2</sub>ONa)Â(CH<sub>2</sub>CH<sub>2</sub>OH)]<sub>2</sub> (<b>2</b>), and the hexanuclear organotin oxo cluster [MeNÂ(CH<sub>2</sub>CH<sub>2</sub>O)<sub>2</sub>SnMe<sub>2</sub>·Me<sub>2</sub>SnO]<sub>3</sub> (<b>3</b>). The compounds were characterized
by <sup>1</sup>H, <sup>13</sup>C, and <sup>119</sup>Sn NMR spectroscopy,
electrospray ionization mass spectrometry, and single-crystal X-ray
diffraction analysis. In the solid state, compound <b>1</b> is
a tetramer that is brought about by intermolecular O→Sn interactions.
In solution, however, it shows a monomer ⇌ dimer equilibrium
that is fast on the <sup>1</sup>H, <sup>13</sup>C, and <sup>119</sup>Sn NMR time scales at room temperature. All compounds show intramolecular
N→Sn interactions at Sn–N distances ranging between
2.378(3) Å (<b>2</b>) and 3.026(3) Å (<b>3</b>·0.25H<sub>2</sub>O). Compound <b>3</b> can formally be
regarded as a molecular dimethyltin oxide being trapped by head-to-tail
complexation with a stannabicyclooctane. In solution, it slowly falls
apart into <b>1</b> and Me<sub>2</sub>SnO