Enantiopure P-Chiral Secondary Phosphines (P*HRR') from the Catalytic Asymmetric Hydrogenation of P═C Bonds.

We report the first bottleable enantiopure P-chiral secondary phosphines from the rhodium-catalyzed asymmetric hydrogenation of phosphaalkenes. Catalytic asymmetric hydrogenation, a reaction of broad academic and industrial importance for C═C, N═C, and O═C bonds, has not previously been reported for the P═C bond. The hydrogenation of ArP═CR2 (Ar = Mes, m-Xyl and TMOP; R = Ph, 4-C6H4F) affords four unprecedented P-stereogenic secondary phosphines in 76%-90% isolated yields with 91%-97% enantiomeric excess (ee). These isolable P-chiral secondary phosphines are configurationally stable indefinitely in the solid state and show only modest loss in ee when kept in solution for over a month at room temperature.

Probing Radical Addition to 1-Phosphabutadienes by Employing Muonium as a "Light Isotope" of Hydrogen.

Understanding free radical addition to multiple bonds is important to elucidating the mechanistic details of addition polymerization reactions, albeit the fleeting radical intermediates are very difficult to detect by conventional methodologies. Muon spin spectroscopy (µSR) is a highly sensitive method that can detect radical species at 106 spins (cf. EPR: 1012 spins, NMR: 1018 spins). Herein, we employ µSR to detect the radical-addition products from three 1-phosphabutadiene monomers, P-analogues of isoprene. We show that muonium (Mu), a "light" H-atom surrogate, adds predominantly at the C4 position of the P1 =C2 -C3 =C4 moiety to give unprecedented 1-phosphaallyl radicals as the major products. Our structural assignments are supported by assignment of muon, phosphorus and proton hyperfine coupling constants using DFT-calculations. A minor radical product is also detected that is tentatively assigned to an PC3 -heterocyclic free radical. On the basis of DFT-predictions, we speculate that its formation may involve initial addition of Mu+ at the C3 position followed by electron capture. These studies provide rare insights into the prospective radical (or cationic) polymerization of 1-phosphabutadienes, which have previously been polymerized using anionic initiation.

Cationic Phosphinidene as a Versatile P1 Building Block: [LC-P]+ Transfer from Phosphonio-Phosphanides [LC-P-PR3]+ and Subsequent LC Replacement Reactions (LC = N-Heterocyclic Carbene).

Cationic imidazoliumyl(phosphonio)-phosphanides [LC-P-PR3]+ (1a-e+, LC = 4,5-dimethyl-1,3-diisopropylimidazolium-2-yl; R = alkyl, aryl) are obtained via the nucleophilic fragmentation of tetracationic tetraphosphetane [(LC-P)4][OTf]4 (2[OTf]4) with tertiary phosphanes. They act as [LC-P]+ transfer reagents in phospha-Wittig-type reactions, when converted with various thiocarbonyls, giving unprecedented cationic phosphaalkenes [LC-P═CR2]+ (5a-f[OTf]) or phosphanides [LC-P-CR(NR2')]+ (6a-d[OTf]). Theoretical calculations suggest that three-membered cyclic thiophosphiranes are crucial intermediates of this reaction. To test this hypothesis, treatment of [LC-P-PPh3]+ with phosphaalkenes, that are isolobal to thioketones, permits the isolation of diphosphirane salts 11a,b[OTf]. Furthermore, preliminary studies suggest that the cationic phosphaalkene [LC-P═CPh2]+ may be employed to access rare examples of η2-P═C π-complexes with Pd0 and Pt0 when treated with [Pd(PPh3)4] and [Pt(PPh3)3] for which analogous complexes of neutral phosphaalkenes are scarce. The versatility of [LC-P]+ as a valuable P1 building block was showcased in substitution reactions of the transferred LC-substituent using nucleophiles. This is demonstrated through the reactions of 5a[OTf] and 6c[OTf] with Grignard reagents and KNPh2, providing a convenient, high-yielding access to MesP═CPh2 (16) and otherwise difficult-to-synthesize 1,3-diphosphetane 17 and P-aminophosphaalkenes.

Ambient Temperature Carbene-Mediated Depolymerization: Stoichiometric and Catalytic Reactions of N-Heterocyclic- and Cyclic(Alkyl)Amino Carbenes with Poly(N-Methylaminoborane) [MeNH-BH2]n.

The reactions of the N-heterocyclic carbenes (NHCs) IDipp and ItBu and the cyclic(alkyl)amino carbene (CAAC) CAACMe with polyaminoborane [MeNH-BH2]n were investigated. Stoichiometric quantities of each carbene were found to cause rapid and complete depolymerization, with the major B-N-containing product identified as the NHC-aminoborane adduct, IDipp-BH2NMeH (1), cyclic borazane [MeNH-BH2]3, or borazine [MeNBH]3 with IDipp, ItBu, and CAACMe, respectively. With substoichiometric quantities of IDipp and ItBu (down to 10 and 2.5 mol %, respectively), complete loss of high molar mass material was also detected, indicating that the depolymerization is catalytic. The main products of the reaction with substoichiometric IDipp were IDipp-BH2NMeH (1) and [MeNH-BH2]3 and with substoichiometric ItBu, [MeNH-BH2]3, and [MeNBH]3 with product ratios dependent on the quantity of NHC used. Under analogous conditions with CAACMe, high molar mass material persisted alongside the formation of [MeNBH]3. Further reactivity studies with cyclic borazane [MeNH-BH2]3 and MeNH2·BH3 provided insights into depolymerization pathways. IDipp showed no reactivity toward [MeNH-BH2]3, whereas with 3 equiv of ItBu and CAACMe, the dehydrogenation product [MeNBH]3, was formed. With MeNH2·BH3, 2 equiv of carbene were used as the first acts to accept dihydrogen; the major products with IDipp, ItBu, and CAACMe were IDipp-BH2NMeH (1), [MeNBH]3, and (CAACMeH)HB═NMeH (2), respectively. The double E-H (E = B, N) bond activation product (CAACMeH)HB═NMe(HCAACMe) (3) was isolated from the reaction between 3 equiv of CAACMe and MeNH2·BH3. A unified mechanism for donor-mediated depolymerization of [MeHN-BH2]n is proposed.

Metathesis of P=C Bonds Catalyzed by N-Heterocyclic Carbenes.

The catalytic metathesis of C=C bonds is a textbook reaction that has no parallel in the widely studied area of multiple bonds involving heavier p-block elements. A high-yielding P=C bond metathesis of phosphaalkenes (ArP=CPh2 , Ar=Mes, o-Tol, Ph) has been discovered that is catalyzed by N-heterocyclic carbenes (NHC=Me2 IMe, Me2 Ii Pr). The products are cyclic oligomers formally derived from ArP=PAr [i. e. cyclo-(ArP)n ; n=3, 4, 5, 6] and Ph2 C=CPh2 . Preliminary mechanistic studies of this remarkable transformation have established NHC=PAr (Ar=Mes, o-Tol, Ph) as key phosphinidene transfer agents. In addition, novel cyclic intermediates, such as, cyclo-(ArP)2 CPh2 and cyclo-(ArP)4 CPh2 have also been observed. This work represents a rare application of non-metal-based catalysts for transformations involving main-group elements.

A Smart Phosphine-Diyne Polymer Displays "Turn-On" Emission with a High Selectivity for Gold(I/III) Ions.

A polymeric phosphine sensor is reported that exhibits bright blue fluorescence in the presence of gold(I/III) ions but is nonemissive with other metal ions. Specifically, solutions of a poly(p-arylenediethynylene phosphine) copolymer are 35 or 94 times more emissive when treated with solutions of (tht)AuCl or HAuCl4·3H2O, respectively. Model compound studies confirm phosphine coordination to metals, including gold(I/III) and rhodium(I), and the selective "turn-on" fluorescence was investigated using time-dependent density functional theory calculations.

Isolable Phosphaalkenes Bearing 2,4,6-Trimethoxyphenyl and 2,6-Bis(trifluoromethyl)phenyl as P-Substituents.

The multistep synthesis and characterization of new P═C analogues of olefins from readily available starting materials is reported. Specifically, the phosphaalkenes TMOP-P═CPh2 (1a: TMOP = 2,4,6-trimethoxyphenyl) and ArF-P═CPh2 [1b: ArF = 2,6-bis(trifluoromethyl)phenyl] have been prepared, isolated, and characterized. In addition, synthetically challenging intermediates, such as the corresponding pyrophoric primary phosphines and bis(trimethylsilyl)phosphines, have been isolated and characterized. The title compounds, TMOP-P═CPh2 (1a) and ArF-P═CPh2 (1b), along with TMOP-PH2 (3a) have been characterized by X-ray crystallography. Importantly, the successful synthesis and isolation of phosphaalkenes 1a and 1b provides a foundation for future investigations of their polymerization, by analogy to the known polymerization of Mes-P═CPh2.

Ammonium and Potassium Salts of a Hexacoordinate Phosphorus(V) Anion Featuring P-O and P-C Bonds.

Ammonium and potassium salts featuring the chiral mer-[P(C6H4CO2)3]-, mer-[1]-, have been isolated. Specifically, treating phosphorane P(C6H4CO2)2(C6H4CO2H), 2, with N-containing bases [Nbase = PhNMe2, PhNH2, pyridine (py), isoquinoline, (-)-brucine, N( n-C8H17)3] afforded ammonium salts [NbaseH]+- mer-[1]-. Each compound was fully characterized spectroscopically, and four were subjected to X-ray crystallographic analysis. Salts were isolated with the racemic mixture of the mer-[1]- anion except in the case of [(-)-brucineH]-Λ- mer-[1], for which the crystal analyzed was enantiomerically pure. The potassium salt, K- mer-[1], was synthesized by treating 2 with KH. The solid-state structure of K- mer-[1] is a coordination polymer consisting of seven- and eight-coordinate K+ ions that are weakly bound by oxygen of either the racemic anion or the methanol solvent. Preliminary NMR and MS data for the formation of the Brønsted acid, H(DMF) n[1], has also been obtained. An estimate of the basicity of anion mer-[1]- was obtained from IR measurements of the N-H stretching frequency for [( n-C8H17)3NH]- mer-[1]. On the basis of these measurements, anion mer-[1]- was ranked similar to the classical weakly coordinating anion, [ClO4]-, in terms of its coordinating ability.

Free Radical Reactivity of a Phosphaalkene Explored Through Studies of Radical Isotopologues.

Muonium (Mu), an H atom analogue, is employed to probe the addition of free radicals to the P=C bond of a phosphaalkene. Specifically, two unprecedented muoniated free radicals, MesP. -CMu(Me)2 (1 a, minor product) and MesPMu-C. Me2 (1 b, major product), were detected by muon spin spectroscopy (µSR) when a solution of MesP=CMe2 (1: Mes=2,4,6-trimethylphenyl) was exposed to a beam of positive muons (µ+ ). The µ+ serves as a source of Mu (that is, Mu=µ+ +e- ). To confirm the identity of the major product 1 b, its spectral features were compared to its isotopologue, MesPH-C. (Me)CH2 Mu (2 a). Conveniently, 2 a is the sole product of the reaction of MesPH(CMe=CH2 ) (2) with Mu. For all observed radicals, muon, proton, and phosphorus hyperfine coupling constants were determined by µSR and compared to DFT-calculated values.

Phosphorus-Containing Block Copolymers from the Sequential Living Anionic Copolymerization of a Phosphaalkene with Methyl Methacrylate.

Although living polymerization methods are widely applicable to organic monomers, their application to inorganic monomers is rare. For the first time, we show that the living poly(methylenephosphine) (PMPn - ) anion can function as a macroinitiator for olefins. Specifically, the phosphaalkene, MesP=CPh2 (PA), and methyl methacrylate (MMA) can be sequentially copolymerized using the BnLi-TMEDA initiator system in toluene. A series of PMPn -b-PMMAm copolymers with narrow dispersities are accessible (D=1.05-1.10). Analysis of the block copolymers provided evidence for -P-CPh2 -CH2 -CMe(CO2 Me)- switching groups. Importantly, this indicates that the -P-CPh2 - anion directly initiates the anionic polymerization of MMA and stands in stark contrast to the isomerization mechanism followed for the homopolymerization of PA. For the first time, the glass transition of a PMPn homopolymer has been measured (Tg =45.1 °C, n=20). The PMPn -b-PMMAm copolymers do not phase separate and show a single Tg which increases with higher PMMA content.

Polymers and the p-block elements.

A survey of the state-of-the-art in the development of synthetic methods to incorporate p-block elements into polymers is given. The incorporation of main group elements (groups 13-16) into long chains provides access to materials with fascinating chemical and physical properties imparted by the presence of inorganic groups. Perhaps the greatest impedance to the widespread academic and commercial use of p-block element-containing macromolecules is the synthetic challenge associated with linking inorganic elements into long chains. In recent years, creative methodologies have been developed to incorporate heteroatoms into polymeric structures, with perhaps the greatest advances occurring with hybrid organic-inorganic polymers composed of boron, silicon, phosphorus and sulfur. With these developments, materials are currently being realized that possess exciting chemical, photophysical and thermal properties that are not possible for conventional organic polymers. This review focuses on highlighting the most significant recent advances whilst giving an appropriate background for the general reader. Of particular focus will be advances made over the last two decades, with emphasis on the novel synthetic methodologies employed.

Polymerization of 1-Phosphaisoprene: Synthesis and Characterization of a Chemically Functional Phosphorus Version of Natural Rubber.

Macromolecules derived from 1,3-dienes, such as polyisoprene (or natural rubber), are of considerable importance in polymer science. Given the parallels between P=C and C=C bonds, the prospect of polymerizing P-containing 1,3-dienes, such as 1-phosphaisoprene, is intriguing due to the unique chemical functionality imparted by the heavier element combined with their structural relationship to natural rubber. Herein, we report the synthesis, characterization and coordination chemistry of the first polymers derived from Mes*P=CR-CH=CH2 (Mes*=2,4,6-t-Bu3 C6 H2 ; R=H, Me). In the case of 1-phosphaisoprene (R=Me), the monomer is isolable and its anionic polymerization affords a polymer that retains P=C bonds in its microstructure. The chemical functionality of these novel materials is demonstrated by forming the macromolecular gold(I) complex where the P=C bond is retained for further chemical elaboration.

Homo- and Heteropolynuclear Complexes Containing Bidentate Bridging 4-Phosphino-N-Heterocyclic Carbene Ligands.

The abnormal reaction of phosphaalkenes with N-heterocyclic carbenes (NHC) offers a convenient method to introduce new functionality at the backbone of an NHC. The 4-phosphino-substituted NHC (1a) derived from 1,3-dimesitylimidazol-2-ylidene (IMes) and MesP═CPh2 is shown to be an effective bifunctional ligand for Au(I) and Pd(II). Several new complexes are reported: 2a: 1a·AuCCl, 3a: 1a·(AuCl)2, 4a: [(1a)2AuC]Cl, 5a: [(1a·AuPCl)2AuC]Cl], and 6a: 1a·(PdC) (AuPCl). The reaction of 4-phosphino-NHC 1b, derived from 1,3-di(cyclohexyl)imidazol-2-ylidene (ICy) and MesP═C(4-C6H4F)2, with (tht)AuCl (2 equiv, tht = tetrahydrothiophene) affords the fascinating tetranuclear 5b [(1b·AuPCl)2AuC][AuCl2]. The molecular structure of 5b features a close Au···Au contact (3.0988(4) Å) between the bis(carbene)gold(I) cation and the dichloroaurate(I) anion. The buried volumes (%Vbur) and Tolman cone angles for representative 4-phosphino-NHCs calculated from structural data are compared to related carbenes and phosphines. The molecular structures are reported for complexes 3a, 4a, 5b, and 6a.

Copper(I) Complexes of Pyridine-Bridged Phosphaalkene-Oxazoline Pincer Ligands.

The synthesis of enantiomerically pure pyridine-bridged phosphaalkene-oxazolines ArP═C(Ph)(2,6-C5H3NOx) (1, Ar = Mes/Mes*, Ox = CNOCH(i-Pr)CH2/CNOCH(CH2Ph)CH2) is reported. This new ligand forms a κ(P), κ(2)(NN) dimeric complex with copper(I) (7) that dissociates into a cationic κ(3)(PNN) monomeric complex upon addition of a neutral ligand {[1a·CuL]OTf (8a-e): L = PPh3 (a), P(OPh)3 (b), 2,6-lutidine (c), 4-DMAP (d), 1-methylimidazole (e)}. The P-Cu bond lengths in 8 are influenced by the π-accepting/σ-donating properties of L, and this can be observed by changes in the δ(31)PP═C NMR shift. The donor-acceptor properties in complexes of type 8 have also been investigated by UV/vis spectroscopy and density functional theory calculations.

Strong Evidence of a Phosphanoxyl Complex: Formation, Bonding, and Reactivity of Ligated Phosphorus Analogues of Nitroxides.

Facile access to [W(CO)5 (Ph2 P-OTEMP)] is used to initiate a study on the generation, properties, and reactions of transient phosphanoxyl complexes [MLn (R2 PO)], the first example of which could be trapped via heterocoupling with the trityl radical. It is also demonstrated that the phosphorus nitroxyl complex acts as radical initiator in the polymerization of styrene. The quest for P-O versus O-N bond homolysis, as well as the initial steps of the polymerization were studied by DFT methods.

Poly(p-phenylenediethynylene phosphane): A Phosphorus-Containing Macromolecule that Displays Blue Fluorescence Upon Oxidation.

Despite the challenges associated with their synthesis, hybrid inorganic-organic polymers featuring heavier main-group elements spaced by π-conjugated organic functionalities have garnered considerable recent attention due to their chemical functionality and novel photophysical properties. We have succeeded in the preparation of an unprecedented organophosphorus polymer possessing functional phosphane-di-yne moieties in the main chain. Namely, poly(p-phenylenediethynylene phosphane) (PPYP) is prepared using a nickel(II)-catalyzed P-C bond-forming reaction. The hexyl-substituted PPYPs are solution processible and have been thoroughly characterized (molecular weight, Mw, ca. 10(4) Da vs. polystyrene; degree of polymerization, DP, ca. 10). Remarkably, although PPYP shows very weak emission upon irradiation with UV light, its oxide shows blue "turn-on" fluorescence. The present discovery bridges the areas of main-group and polymer science and opens the door to a new class of σ-π-conjugated macromolecules with unique chemical functionality.

H(OEt2)2[P(1,2-O2C6Cl4)3]: synthesis, characterization, and application as a single-component initiator for the carbocationic polymerization of olefins.

The development of novel Brønsted acids featuring the hexacoordinate phosphorus(V) anion [TRISPHAT](-) {[1](-)=[P(1,2-O2C6Cl4)3](-)} are reported. The title compound, H(OEt2)2[1], was synthesized from 1,2-(HO)2C6Cl4 (3 equiv) and PCl5 in the presence of diethyl ether. This compound was fully characterized by (1)H, (31)P and (13)C NMR spectroscopy, X-ray crystallography and elemental microanalysis. Dissolution of H(OEt2)2[1] in acetonitrile results in the slow precipitation of crystalline H(OEt2)(NCMe)[1], which was characterized by X-ray diffraction; however, in CD2Cl2 solution the [TRISPHAT](-) anion protonated and ring-opened. The weighable, solid H(OEt2)2[1] was found to be a competent initiator for the polymerization of n-butyl vinyl ether, α-methylstyrene, styrene and isoprene at a variety of temperatures and monomer-to-initiator ratios. At low temperatures, polymers with M(n) >10(5) were obtained for n-butyl vinyl ether and α-methylstyrene whereas slightly lower molecular weights were obtained with styrene and isoprene (10(4) < M(n) <10(5)). The poly(α-methylstyrene) synthesized at -78 °C is syndiotactic-rich (ca. 87% rr) whereas the polystyrene obtained at -50 °C is atactic. The polyisoprene obtained possessed all possible modes of enchainment as well as branched and/or cyclic structures that are often observed in polyisoprene.

Synthesis of an imidazolium phosphanide zwitterion and its conversion into anionic imidazol-2-ylidene derivatives.

Matter of opinion: The novel zwitterion 1 has been synthesized and studied theoretically and also converted into anionic NHCs 2. The former can also be described as a phosphinidene adduct of an abnormal N-heterocyclic carbene (1') and, in the same vein, the latter represents a phosphinidene adduct of an anionic N-heterocyclic dicarbene (2').

P=C bonds as building blocks for three- and four-membered heterocyclic cations: synthesis, structures and mechanistic studies.

The activation of the P=C bond of phosphaalkenes with electrophiles is investigated as a means to prepare and characterize unusual organophosphorus compounds. Treatment of RP=CHtBu (1a: R=tBu; 1b: R=1-adamantyl) with HOTf (0.5 equiv) affords diphosphiranium salts [RP-CHtBu-PR (CH(2)tBu)]OTf ([2a]OTf and [2b]OTf), each containing a three-membered P(2)C ring. In contrast, the addition of MeOTf (0.5 equiv) to either 1a or 1b affords diphosphetanium salts [RP-CHtBu-P(Me)R-CHtBu]OTf ([3a]OTf and [3b]OTf) containing four-membered P(2)C(2) heterocycles. The phosphenium triflate [tBuP(CH(2)tBu)]OTf ([5a]OTf) and methylenephosphonium triflate [tBu(Me)P=CHtBu]OTf ([7a]OTf) are identified spectroscopically as intermediates in the formation of [2a](+) and [3a](+), respectively. The phosphenium triflate intermediate can be trapped with 2-butyne to afford phosphirenium salt [MeC=CMe-tBuPCH(2)tBu]OTf ([6a]OTf). Treatment of diphosphetanium [3a]OTf with an excess MeOTf affords [Me(2)P-CHtBu-PMetBu-CHtBu](OTf)(2) ([4a](OTf)(2)), a compound containing a diphosphetanium dication. The molecular structures are reported for [2a]OTf, [2b][H(OTf)(2)], [3a]I, [3b]I, [4a](OTf)(2), and [6a]OTf.

Enantiomerically pure phosphaalkene-oxazolines (PhAk-Ox): synthesis, scope and copolymerization with styrene.

The design of a synthetic route to a class of enantiomerically pure phosphaalkene-oxazolines (PhAk-Ox) is presented. The condensation of a lithium silylphosphide and a ketone (the phospha-Peterson reaction) was used as the P=C bond-forming step. Attempted condensation of PhC(=O)Ox (Ox = CNOCH(iPr)CH(2)) and MesP(SiMe(3))Li gave the unusual heterocycle (MesP)(2)C(Ph)=CN-(S)-CH(iPr)CH(2)O (3). However, PhAk-Ox (S,E)-MesP=C(Ph)CMe(2)Ox (1 a) was successfully prepared by treating MesP(SiMe(3))Li with PhC(=O)CMe(2)Ox (52 %). To demonstrate the modularity and tunability of the phospha-Peterson synthesis several other phosphaalkene-oxazolines were prepared in an analogous manner to 1 a: TripP=C(Ph)CMe(2)Ox (1 b; Trip = 2,4,6-triisopropylphenyl), 2-iPrC(6)H(4)P=C(Ph)CMe(2)Ox (1 c), 2-tBuC(6)H(4)P=C(Ph)CMe(2)Ox (1 d), MesP=C(4-MeOC(6)H(4))CMe(2)Ox (1 e), MesP=C(Ph)C(CH(2))(4)Ox (1 f), and MesP=C(3,5-(CF(3))(2)C(6)H(3))C(CH(2))(4)Ox (1 g). To evaluate the PhAk-Ox compounds as prospective precursors to chiral phosphine polymers, monomer 1 a and styrene were subjected to radical-initiated copolymerization conditions to afford [{MesPC(Ph)(CMe(2)Ox)}(x){CH(2)CHPh}(y)](n) (9 a: x = 0.13n, y = 0.87n; GPC: M(w) = 7400 g mol(-1) , PDI = 1.15).