1979
DOI: 10.1021/ja00511a022
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A tris(dialkylamino)phosphine with pyramidal nitrogens

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Cited by 39 publications
(26 citation statements)
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“…Acetone (Me 2 CO) was stirred over B 2 O 3 for at least 24 h, distilled, and finally degassed by purging with Argon. [60] Literature known procedures were employed to synthesize the macrocyclic amine side-arm, 1,4-diisopropyl-1,4,7-triazacyclononane, [61,62] and the bridging unit, 3,5-bis(chlorocarbonyl)-1H-pyrazole, [63] used to prepare HL Am .…”
Section: General Materials and Methodsmentioning
confidence: 99%
“…Acetone (Me 2 CO) was stirred over B 2 O 3 for at least 24 h, distilled, and finally degassed by purging with Argon. [60] Literature known procedures were employed to synthesize the macrocyclic amine side-arm, 1,4-diisopropyl-1,4,7-triazacyclononane, [61,62] and the bridging unit, 3,5-bis(chlorocarbonyl)-1H-pyrazole, [63] used to prepare HL Am .…”
Section: General Materials and Methodsmentioning
confidence: 99%
“…while the coordination of the N sites was never observed.8 A forced pyramidal configuration at nitrogen does not guarantee obtaining a stable adduct at nitrogen. 21 The behavior of the bicyclic aminophosphanes 1 (Scheme 11) is therefore of interest. Although the P-adduct 10 is still the first to form, dicoordination to yield 11 readily takes place when a second equivalent of BH, is added (unless there is, as in Id, steric hindrance at nitr~gen).…”
Section: Protonation and Alkylationmentioning
confidence: 99%
“…This tridentate ligand, connected to a Cu II central atom, promotes mainly fivecoordination (Han et al, 2004;Wang et al, 2004), thus leaving two coordination sites free for the polymerization process during crystallization. As a result of our synthetic procedure using tacnÁ3HBr, prepared according to the literature (White et al, 1979), we have isolated the title compound, (I).…”
Section: Commentmentioning
confidence: 99%