Abstract Photolyses oftrans‐Fe(CO)3(P((CH2)n)3P) (n=10 (a), 12 (b), 14 (c), 16 (d), 18 (e)) in the presence of PMe3provide the first economical and scalable route to macrobicyclic dibridgehead diphosphines P((CH2)n)3P (1). These are isolated as mixtures ofin,in/out,outisomers that equilibrate with degeneratein,out/out,inisomers at 150 °C via pyramidal inversion at phosphorus. For the entire series, VT31P NMR data establish or boundKeq, rates, and activation parameters for a variety of phenomena, many of which involve homeomorphic isomerizations, topological processes by which certain molecules can turn themselves inside out (e. g.,in,in⇌out,out). This provides the first detailed mapping of such trends in homologous series of aliphatic bicyclic compounds XE((CH2)n)3EX with any type of bridgehead. Isomeric diborane adducts1 a,d ⋅ 2BH3are also characterized. Crystal structures ofout,out‐1 aandin,in‐1 a ⋅ 2BH3aid isomer assignments and reveal unusual cage conformations.
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Syntheses, homeomorphic and configurational isomerizations, and structures of macrocyclic aliphatic dibridgehead diphosphines; molecules that turn themselves inside out
The diphosphine complexes cis - or trans -PtCl 2 (P((CH 2 ) n ) 3 P) ( n = b/12, c/14, d/16, e/18) are demetalated by MCX nucleophiles to give the title compounds (P((CH 2 ) n ) 3 )P (3b–e, 91–71%). These “empty cages” react with PdCl 2 or PtCl 2 sources to afford trans -MCl 2 (P((CH 2 ) n ) 3 P). Low temperature 31 P NMR spectra of 3b and c show two rapidly equilibrating species (3b, 86 : 14; 3c, 97 : 3), assigned based upon computational data to in , in (major) and out , out isomers. These interconvert by homeomorphic isomerizations, akin to turning articles of clothing inside out (3b/c: Δ H ‡ 7.3/8.2 kcal mol −1 , Δ S ‡ −19.4/−11.8 eu, minor to major). At 150 °C, 3b, c, e epimerize to (60–51) : (40–49) mixtures of ( in , in / out , out ) : in , out isomers, which are separated via the bis(borane) adducts 3b, c, e·2BH 3 . The configurational stabilities of in , out -3b, c, e preclude phosphorus inversion in the interconversion of in , in and out , out isomers. Low temperature 31 P NMR spectra of in , out -3b, c reveal degenerate in , out / out , in homeomorphic isomerizations (Δ G ‡Tc 12.1, 8.5 kcal mol −1 ). When ( in , in / out , out )-3b, c, e are crystallized, out , out isomers are obtained, despite the preference for in , in isomers in solution. The lattice structures are analyzed, and the D 3 symmetry of out , out -3c enables a particularly favorable packing motif. Similarly, ( in , in / out , out )-3c, e·2BH 3 crystallize in out , out conformations, the former with a cycloalkane solvent guest inside.
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- Award ID(s):
- 1900549
- PAR ID:
- 10435569
- Date Published:
- Journal Name:
- Chemical Science
- Volume:
- 13
- Issue:
- 45
- ISSN:
- 2041-6520
- Page Range / eLocation ID:
- 13368 to 13386
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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