Cobalt-Mediated [3+1] Fragmentation of White Phosphorus: Access to Acylcyanophosphanides.

Despite the accessibility of numerous transition metal polyphosphido complexes through transition-metal-mediated activation of white phosphorus, the targeted functionalization of Pn ligands to obtain functional monophosphorus species remains challenging. In this study, we introduce a new [3+1] fragmentation procedure for cyclo-P4 ligands, leading to the discovery of acylcyanophosphanides and -phosphines. Treatment of the complex [K(18c-6)][(Ar*BIAN)Co(η4 -P4 )] ([K(18c-6)]3, 18c-6=[18]crown-6, Ar*=2,6-dibenzhydryl-4-isopropylphenyl, BIAN=1,2-bis(arylimino)acenaphthene diimine) with acyl chlorides results in the formation of acylated tetraphosphido complexes [(Ar*BIAN)Co(η4 -P4 C(O)R)] (R=tBu, Cy, 1-Ad, Ph; 4 a-d). Subsequent reactions of 4 a-d with cyanide salts yield acylated cyanophosphanides [RC(O)PCN]- (9 a-d- ) and the cyclo-P3 cobaltate anion [(Ar*BIAN)Co(η3 -P3 )(CN)]- (8- ). Further reactions of 4 a-d with trimethylsilyl cyanide (Me3 SiCN) and isocyanides provide insight into a plausible mechanism of this [3+1] fragmentation reaction, as these reagents partially displace the P4 C(O)R ligand from the cobalt center. Several potential intermediates of the [3+1] fragmentation were characterized. Additionally, the introduction of a second acyl substituent was achieved by treating [K(18c-6)]9b with CyC(O)Cl, resulting in the first bis(acyl)monocyanophosphine (CyC(O))2 PCN (10).

Direct Synthesis of Phosphoryltriacetates from White Phosphorus via Visible Light Catalysis.

Organophosphorus compounds (OPCs) are widely used in many fields. However, traditional synthetic routes in the industry usually involve multistep and hazardous procedures. Therefore, it's of great significance to construct such compounds in an environmentally-friendly and facile way. Herein, a photoredox catalytic method has been developed to construct novel phosphoryltriacetates. Using fac-Ir(ppy)3 (ppy=2-phenylpyridine) as the photocatalyst and blue LEDs (456 nm) as the light source, white phosphorus can react with α-bromo esters smoothly to generate phosphoryltriacetates in moderate to good yields. This one-step approach features mild reaction conditions and simple operational process without chlorination.

Isolation and Reactivity of Homoleptic Diphosphene Lead Complexes.

Due to their limited capacity for π-backdonation, isolation of π-complexes of main-group elements remains a great challenge. We report herein the synthesis of a homoleptic diphosphene lead complex (2) from the degradation of P4 with a bis(germylene)-stabilized Pb(0) complex. Structural and computational studies showed that 2 possesses significant π bonding interactions between Pb atom and diphosphene ligands, which is reminiscent of transition-metal diphosphene complexes. Consistent with its unique electronic structure, complex 2 can deliver Pb(0) atoms to perform redox reaction with an iminoquinone to produce a cyclic plumbylene (4) and perform 2,5-dimethyl-3,4-dimethylimidazol-1-ylidene (IMe2 Me2 ) induced phosphorus cation abstraction to give an anionic PbP3 complex (6).

Cobalt Cyclopentadienyl-Phosphine Dinitrogen Complexes.

By applying the potassium salts of cyclopentadienyl-phosphine ligands LK to CoCl2 , the corresponding cobalt chlorides (1, LCoII Cl) were prepared. By reducing complexes 1 with KHBEt3 under a N2 atmosphere, bridging end-on complexes, LCoI -N2 -CoI L (2 a and 2 b), were successfully obtained. 15 N2 -labeled [15 N2 ]-2 a was prepared under 15 N2 /14 N2 exchange in THF solution. LCoI -N2 -CoI L complex 2 a could react with P4 molecules to release N2 and generate a Co-P4 -Co moiety 4. Further reduction of complex 2 b led to cleavage of a P-C bond in the cyclopentadienyl-phosphine ligand to provide novel µ-PCy2 -bridged Co0 -N2 complex 5. DFT calculations confirmed the experimental observations.

PNP Ligands in Cobalt-Mediated Activation and Functionalization of White Phosphorus.

Transition-metal mediated white phosphorus activation is of high interest as an ecological alternative to P4 chlorination pathway to the practically useful phosphorus products. Herein, we report a facile approach for P4 activation, transformation and subsequent functionalization using cobalt complexes bearing PNP ligands. The use of N,N-bis(diphenylphosphino)amine as a ligand allows one to transform P4 tetrahedron into a zig-zag chain with the formation of complex [Co(Ph2 PNHP(Ph2 )PPPPP(Ph2 )NHPPh2 )]BF4 (4). The presence of organic substituent at nitrogen atom in PNP ligand enables one to obtain complexes with η1 -coordinated P4 molecule, which indicates a crucial role of N-H bond in transformation of white phosphorus tetrahedron. Additionally, complex 4 can readily be functionalized by means of the reaction with Ph2 PCl leading to the formation of a new complex bearing unique P9 -ligand. The obtained results provide opportunities for facile construction of new polyphosphorus ligands in the coordination sphere of transition metal complexes.

Selective [2+1+1] Fragmentation of P4 by heteroleptic Metallasilylenes.

Small-molecule activation by low-valent main-group element compounds is of general interest. We here report the synthesis and characterization (1 H, 13 C, 29 Si NMR, IR, sc-XRD) of heteroleptic metallasilylenes L1 (Cl)MSiL2 (M=Al 1, Ga 2, L1 =HC[C(Me)NDipp]2 , Dipp=2,6-i Pr2 C6 H3 ; L2 =PhC(Nt Bu)2 ). Their electronic nature was analyzed by quantum chemical computations, while their promising potential in small-molecule activation was demonstrated in reactions with P4 , which occurred with unprecedented [2+1+1] fragmentation of the P4 tetrahedron and formation of L1 (Cl)MPSi(L2 )PPSi(L2 )PM(Cl)L1 (M=Al 3, Ga 4).

d/f-Polypnictides Derived by Non-Classical Ln2+ Compounds: Synthesis, Small Molecule Activation and Optical Properties.

Reduction chemistry induced by divalent lanthanides has been primarily focused on samarium so far. In light of the rich physical properties of the lanthanides, this limitation to one element is a drawback. Since molecular divalent compounds of almost all lanthanides have been available for some time, we used one known and two new non-classical reducing agents of the early lanthanides to establish a sophisticated reduction chemistry. As a result, six new d/f-polyphosphides or d/f-polyarsenides, [K(18-crown-6)] [Cp''2 Ln(E5 )FeCp*] (Ln=La, Ce, Nd; E=P, As) were obtained. Their reactivity was studied by activation of P4 , resulting in a selective expansion of the P5 rings. The obtained compounds [K(18-crown-6)] [Cp''2 Ln(P7 )FeCp*] (Ln=La, Nd) are the first examples of an activation of P4 by a f-element-polypnictide complex. Additionally, the first systematic femtosecond (fs)-spectroscopy investigations of d/f-polypnictides are presented to showcase the advantages of having access to a broader series of lanthanide compounds.

Reversible Activation and Transfer of White Phosphorus by Silyl-Stannylene.

Use of a silyl supported stannylene (Mes TerSn(Sit Bu3 ) [Mes Ter=2,6-(2,4,6-Me3 C6 H2 )2 C6 H3 ] enables activation of white phosphorus under mild conditions, which is reversible under UV light. The reaction of a silylene chloride with the activated P4 complex results in facile P-atom transfer. The computational analysis rationalizes the electronic features and high reactivity of the heteroleptic silyl-substituted stannylene in contrast to the previously reported bis(aryl)stannylene.

The Butterfly Complex [{Cp*Cr(CO)3 }2 (µ,η1:1 -P4 )] as a Versatile Ligand and Its Unexpected P1 /P3 Fragmentation.

The versatile coordination behavior of the P4 butterfly complex [{Cp*Cr(CO)3 }2 (µ,η1:1 -P4 )] (1) towards Lewis acidic pentacarbonyl compounds of Cr, Mo and W is reported. The reaction of 1 with [W(CO)4 (nbd)] (nbd=norbornadiene) yields the complex [{Cp*Cr(CO)3 }2 (µ3 ,η1:1:1:1 -P4 ){W(CO)4 }] (2) in which 1 serves as a chelating P4 butterfly ligand. In contrast, reactions of 1 with [M(CO)4 (nbd)] (M=Cr (a), Mo (b)) result in the step-wise formation of [{Cp*Cr(CO)2 }2 (µ3 ,η3:1:1 -P4 ){M(CO)5 }] (3 a,b) and [{Cp*Cr(CO)2 }2 -(µ4 ,η3:1:1:1 -P4 ){M(CO)5 }2 ] (4 a,b) which contain a folded cyclo-P4 unit. Complex 4 a undergoes an unprecedented P1 /P3 -fragmentation yielding the cyclo-P3 complex [Cp*Cr(CO)2 (η3 -P3 )] (5) and the as yet unknown phosphinidene complex [Cp*Cr(CO)2 {Cr(CO)5 }2 (µ3 -P)] (6). The identity of 6 is confirmed by spectroscopic methods and by the in situ formation of [{Cp*Cr(CO)2 (tBuNC)}P{Cr(CO)5 }2 (tBuNC)] (7). DFT calculations throw light on the bonding situation of the reported products.

Aggregation and Degradation of White Phosphorus Mediated by N-Heterocyclic Carbene Nickel(0) Complexes.

The reaction of zerovalent nickel compounds with white phosphorus (P4 ) is a barely explored route to binary nickel phosphide clusters. Here, we show that coordinatively and electronically unsaturated N-heterocyclic carbene (NHC) nickel(0) complexes afford unusual cluster compounds with P1 , P3 , P5 and P8 units. Using [Ni(IMes)2 ] [IMes=1,3-bis(2,4,6-trimethylphenyl)imidazolin-2-ylidene], electron-deficient Ni3 P4 and Ni3 P6 clusters have been isolated, which can be described as superhypercloso and hypercloso clusters according to the Wade-Mingos rules. Use of the bulkier NHC complexes [Ni(IPr)2 ] or [(IPr)Ni(η6 -toluene)] [IPr=1,3-bis(2,6-diisopropylphenyl)imidazolin-2-ylidene] affords a closo-Ni3 P8 cluster. Inverse-sandwich complexes [(NHC)2 Ni2 P5 ] (NHC=IMes, IPr) with an aromatic cyclo-P5 - ligand were identified as additional products.

Bi-P Bond Homolysis as a Route to Reduced Bismuth Compounds and Reversible Activation of P4.

Bismuth diphenylphosphanides Bi(NONR )(PPh2 ) (NONR =[O(SiMe2 NR)2 ], R=tBu, 2,6-iPr2 C6 H3 , Aryl) undergo facile decomposition via single-electron processes to form reduced Bi and P species. The corresponding derivatives Bi(NONR )(PCy2 ) are stable. Reaction of the isolated BiII radical . Bi(NONAr ) with white phosphorus (P4 ) proceeds with the reversible and selective activation of a single P-P bond to afford the bimetallic µ,η1:1 -bicyclo[1.1.0]tetraphosphabutane compound.

Probing the Structure, Dynamics, and Bonding of Coinage Metal Complexes of White Phosphorus.

A series of cationic white phosphorus complexes of the coinage metals Au and Cu have been synthesised and characterised both in the solid state and in solution. All complexes feature a P4 unit coordinated through an edge P-P vector (η(2)-like), although the degree of activation (as measured by the coordinated P-P bond length) is greater in the gold species. All of the cations are fluxional on the NMR timescale at room temperature, but in the case of the gold systems fluxionality is frozen out at -90 °C. Electronic structure calculations suggest that this fluxionality proceeds via an η(1)-coordinated M-P4 intermediate.

Attenuated Organomagnesium Activation of White Phosphorus.

Sequential reactions between a 2,6-diisopropylphenyl-substituted ß-diketiminato magnesium n-butyl derivative and P4 allow the highly discriminating synthesis of unusual [nBu2P4](2-) and [nBu2P8](2-) cluster dianions.

Selective functionalization of P4 by metal-mediated C-P bond formation.

A new and selective one-step synthesis was developed for the first activation stage of white phosphorus by organic radicals. The reactions of NaCp(R) with P4 in the presence of CuX or FeBr3 leads to the clean formation of organic substituted P4 butterfly compounds Cp(R)2P4 (Cp(R): Cp(BIG)=C5(4-nBuC6H4)5 (1 a), Cp'''=C5H2tBu3 (1 b), Cp*=C5Me5 (1 c) und Cp(4iPr)=C5HiPr4 (1 d)). The reaction proceeds via the activation of P4 by Cp(R) radicals mediated by transition metals. The newly formed organic derivatives of P4 have been comprehensively characterized by NMR spectroscopy and X-ray crystallography.

Formation of [Bi(11)](3-) , a homoatomic, polycyclic bismuth polyanion, by pyridine-assisted decomposition of [GaBi(3)](2-).

Until now, polycyclic bismuth polyanions have not been known-thus discriminating bismuth from its lighter congeners. However, the synthesis of [K([2.2.2]crypt)]3 (Bi11 )⋅2 py⋅tol, allows us to present the first structurally characterized homoatomic, polycyclic bismuth polyanion, which exhibits the [P11 ](3-) "ufosan" structure. It was obtained upon treatment of [K([2.2.2]crypt)]2 (GaBi3 )⋅en with the solvent pyridine. The binary Zintl anion [GaBi3 ](2-) decomposes under oxidative coupling of pyridine molecules and release of H2 to form the title compound. The unprecedented reaction, its products and by-products were investigated by means of spectroscopy, spectrometry, and DFT studies. All findings reveal the specific reaction conditions to be crucial for the formation of the [Bi11 ](3-) ion-and indicate the possibility of the generation and isolation of further, large bismuth polyanions.