2008
DOI: 10.1002/hc.20397
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1,3,6‐Azadiphosphacycloheptanes: A novel type of heterocyclic diphosphines

Abstract: The novel type

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Cited by 37 publications
(31 citation statements)
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“…After one half of hour two additional sets of signals appeared in the NMR spectra (e.g. 45 The signals of two new components in 1 H and 31 P spectra are situated in the same regions and have the same intensity and multiplicity relationships as in described 7-membered heterocycles 8 suggesting that they have chemically close 50 structure. Intensities of new sets of signals increased with time while the signals ascribed to 14-membered macrocycle diminished.…”
Section: Resultsmentioning
confidence: 98%
“…After one half of hour two additional sets of signals appeared in the NMR spectra (e.g. 45 The signals of two new components in 1 H and 31 P spectra are situated in the same regions and have the same intensity and multiplicity relationships as in described 7-membered heterocycles 8 suggesting that they have chemically close 50 structure. Intensities of new sets of signals increased with time while the signals ascribed to 14-membered macrocycle diminished.…”
Section: Resultsmentioning
confidence: 98%
“…The X-ray structure analysis unambiguously established the configurations of 3 RRS in the solid state ( Figure 4, Table 1), as well as the typical twist-chair conformation of the seven-membered ring. [23] The nitrogen atom is in a pyramidal environment (the sum of the bond angles is 337.81°), and the exocyclic substituent on the nitrogen atom is in an axial position. [23] The nitrogen atom is in a pyramidal environment (the sum of the bond angles is 337.81°), and the exocyclic substituent on the nitrogen atom is in an axial position.…”
Section: Synthesesmentioning
confidence: 94%
“…The seven-membered rings in 3 RSS and 4 RSR exhibit unusual chair conformations with almost planar P-C-C-P fragments [the torsion angles P(3)-C(4)-C(5)-P(6) in 3 RSS and 4 RSR are -2.1 and 8.0°, respectively (Table 1)] with the P-C bonds in eclipsed positions. [23] The nitrogen To the best of our knowledge, up to now stable chair conformations have only been described for cycloheptanes with rigid benzo groups or unsaturated ethene-1,2-diyl fragments linking the phosphorus atoms. The P(3)···P(6) distances are short (3.120 and 3.118 Å for 3 RSS and 4 RSR , respectively) in comparison with P···P distances within known rac isomers of 1-aza-3,6-diphosphacycloheptanes (3.599-3.985 Å).…”
Section: Synthesesmentioning
confidence: 99%
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“…Thus, the meso isomers are chelating P,P-ligands, whereas the racemates are bridging ligands that form oligomeric metal complexes (Scheme 23). 46,50 Scheme 23…”
Section: Construction Of Macrocyclic Polyphosphinesmentioning
confidence: 99%