1989
DOI: 10.1002/9780470132562.ch3
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Tervalent Phosphorus–Nitrogen Ring Compounds

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Cited by 5 publications
(2 citation statements)
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“…Still worse, the reaction no longer forms the desired cage exclusively, but a mixture dominated by RN@P(-NHR) 2 and P(-NHR) 3 [9,10]. A more elaborate preparation is reported for the isopropyl analogue [11]. This report details the synthesis of a new member of the P 4 (NR) 6 family according to a two-step, one-pot preparation method shown in Scheme 2.…”
Section: Introductionmentioning
confidence: 93%
“…Still worse, the reaction no longer forms the desired cage exclusively, but a mixture dominated by RN@P(-NHR) 2 and P(-NHR) 3 [9,10]. A more elaborate preparation is reported for the isopropyl analogue [11]. This report details the synthesis of a new member of the P 4 (NR) 6 family according to a two-step, one-pot preparation method shown in Scheme 2.…”
Section: Introductionmentioning
confidence: 93%
“…The unique chemical versatility of these P–N frameworks – provided by the diversity of their topological arrangements – provides potential in numerous applications [ 92 ]. However, these species remain typically arduous to synthesize and isolate, since phosphazane arrangements are generally highly air- and moisture-sensitive [ 93 94 ], and their halogenated precursors are incompatible with protic solvents. Mechanochemistry therefore offers an elegant synthetic route by circumventing solvent compatibility issues, the tedious processes associated with the use of strict anhydrous solvents, and by minimizing unwanted side-products (see Scheme 6 ) [ 95 ].…”
Section: Reviewmentioning
confidence: 99%