Reactivity of Rare Earth Metal Alkyl Complexes with Nitriles or Isonitrile: Versatile Ways toward Multiply Functionalized ß-Diketiminato, (Iso)indolyl, and Imidazolyl Chelating Rare Earth Metal Complexes.

The reactivity of the rare earth metal alkyl complexes LRE(CH2SiMe3)(THF)2 (1RE) [RE = Y (1Y), Yb (1Yb), Lu (1Lu); L = 2,5-[(2-pyrrolyl)CPh2]2(N-methylpyrrole)] with various nitriles and isonitriles has been fully developed. Treatment of the yttrium monoalkyl complex (1Y) with 2 equiv of aromatic nitriles afforded the symmetric trisubstituted ß-diketiminato yttrium complexes (2Y(H), 2Y(Me), and 2Y(F)) through successive cyano group insertion into the RE-C bond and 1,3-H shift or the unsymmetric trisubstituted ß-diketiminato yttrium complex (3Y) unexpectedly via a 1,3-SiMe3 shift when 4-(trifluoromethyl)benzonitrile was used in this reaction under the same conditions. By treating 1Y with 2 equiv of tolyl acetonitrile, an activation of the sp3 C-H bond occurred to form the corresponding ß-aryl keteniminato complexes 4Y(p-tol) and 4Y(m-tol). Remarkably, a heteroleptic cleavage of the CO-CN bond took place in the reaction of 1Y with benzoyl nitrile, affording the unsymmetric trinuclear yttrium complex 5Y bridged by three cyanide groups. Dinuclear ytterbium and lutetium complexes 6Yb and 6Lu containing a functionalized isoindole fragment were synthesized from the reactions of 1 with phthalonitrile by tandem insertion and cyclization. Further studies indicated that the temperature and stoichiometric ratio have a great influence on the reactivity patterns between the reactions of 1RE with benzylisonitrile: two tetrasubstituted ß-diketiminato complexes 8 and 9 were obtained at -30 °C, and tetrasubstituted imidazolyl yttrium and lutetium complexes 7 were isolated at elevated temperature, respectively. In addition, the tetrasubstituted ß-diketiminato complexes 8 and 9 could be irreversibly converted to the cyclization products 7 by elevating the reaction temperature not only on the NMR scale but also on the preparative scale. Notably, when the phenyl isonitrile instead of benzyl isonitrile was reacted with 1Yb, a 2,3-functionalized indolyl ytterbium complex 10Yb was isolated.

Aryl C-H bond functionalization with diphenyldiazomethane induced by rare-earth metal alkyl complexes.

The first examples of regioselective aryl ortho-C-H functionalization with diphenyldiazomethane for the construction of Caryl-Nhydrazinato bonds were accomplished via the activation of C-H bonds and the subsequent reaction of diphenyldiazomethane with the RE-Caryl bond. The reactions of rare-earth metal monoalkyl complexes LRE(CH2SiMe3)(THF)2 (L = 2,5-[(2-pyrrolyl)CPh2]2(N-Me-pyrrole)) supported by a neutral N-methylpyrrole anchored dipyrrolyl ligand with 2 equiv. of Ph2CN2 gave irreversibly unprecedented hydrazonato-functionalized imino rare-earth metal complexes LRE(Ph2CNNC6H4-(o-CNHPh) (RE = Y (2a), Lu (2a')) in good yields involving a rather complex process including the interaction of a diazo unit with a RE-Calkyl bond, a ß-H elimination, a N-N cleavage, 1,4-hydrogen transfer and the subsequent C-N coupling with another diphenyldiazomethane. More important is that regioselective aryl C-H bond functionalization with diphenyldiazomethane to construct the Caryl-Nhydrazinato bonds can be easily achieved by three-component reactions of rare-earth metal monoalkyl complexes, a wide range of substituted imines (including aldimines, ketimines or analogous 2-phenylpyridine) and diphenyldiazomethane, affording various hydrazonato-functionalized phenyl, thienyl imino or pyridyl rare-earth metal complexes 2b-2j at room temperature. A further study indicated that the substituents on the phenyl ring have a great effect on the reaction pathway and governed the Caryl-Nhydrazinato bond construction. Moreover, the experimental studies show that the formation of the Caryl-Nhydrazinato bonds is thermodynamically facile, which could be realized at room temperature easily.

Rare-Earth Metal Complexes Supported by 1,3-Functionalized Indolyl-Based Ligands for Efficient Hydrosilylation of Alkenes.

Two different 1,3-functionalized indolyl-based proligands 1-(2-C4H7O)CH2-3-(2-tBuC6H5N═CH)C8H5N (HL1) and 1-Me2NCH2CH2-3-(2-iPrC6H5N═CH)C8H5N (HL2) were designed, prepared in high yields, and successfully applied to rare-earth metal chemistry showing different reactivities and different bondings with the central metals. The reactions of HL1 with RE(CH2SiMe3)3(THF)2 provided two types of rare-earth metal complexes: the pincer type mononuclear complexes κ3-(L1)RE(CH2SiMe3)2 [L1 = 1-(2-C4H7O)CH2-3-(2-tBuC6H5N═CH)C8H4N, RE = Lu(1), Yb(2)], and the dinuclear rare-earth metal alkyl (per alkyl/per metal) complexes having the ligand in novel coordination modes {(η1:(µ-η2:η1):η1-1-(2-C4H7O)CH2-3-[2-tBuC6H5NCH-(CH2SiMe3)]C8H4N)RECH2SiMe3}2 [RE = Er(3), Y(4), Dy(5), and Gd(6)]. Meanwhile, the reactions of HL2 with RE(CH2SiMe3)3(THF)2 led to the isolation and characterization of only the mononuclear rare-earth metal dialkyl complexes κ3-(L2)RE(CH2SiMe3)2 [L2 = 1-Me2NCH2CH2-3-(2-iPrC6H5N═CH)C8H4N, RE = Lu(7), Gd(8)] bearing the ligand in the pincer chelate form. The mononuclear complexes were formed through the sp2 C-H activation of the 2-indolyl moiety, while the dinuclear complexes were produced unexpectedly through the tandem 2-indolyl sp2 C-H activation and C═N insertion into the RE-CH2SiMe3 bond. These complexes were fully characterized by spectroscopic methods, elemental analyses, and single-crystal X-ray crystallography. The applications of the synthesized complexes as catalysts for the hydrosilylation of terminal alkenes with phenylsilane are described. Anti-Markovnikov addition products were produced by the hydrosilylation of aliphatic olefins, and Markovnikov addition products were isolated with aromatic olefins with high selectivity in the absence of cocatalysts. It is found that the dinuclear rare-earth alkyl complexes exhibited the best catalytic activity with the advantages of mild reaction conditions, short reaction time, low catalyst loading, and wide substrate applicability in comparison with the synthesized mononuclear complexes and the reported catalysts.

Halide-bridged tetranuclear organocopper(I) clusters supported by indolyl-based NCN pincer ligands and their catalytic activities towards the hydrophosphination of alkenes.

Novel tetranuclear organocopper(I) clusters bridged by two halides and two indolyl-based NCN pincer ligands were synthesized through the reactions of Cu(I) halides with lithiated ligands. Single-crystal X-ray diffraction revealed that the structure of these complexes included a [Cu4X2]2+ cluster unit wherein the four copper ions were stabilized by multiple Cu-Cu interactions, arranged in a distorted tetrahedral fashion and the halide anions µ3-bridged with metal centers. Meanwhile, these clusters displayed excellent catalytic activities towards the hydrophosphination of alkenes under solvent-free conditions with wide functional group tolerance.

Indolyl-based Copper(I) Complex-Catalyzed Intermolecular Trifluoromethylazolation of Alkenes via Radical Process.

Herein, we synthesized and characterized a binuclear copper(I) complex supported by the indolyl-based ligand. Employing this complex as catalyst, we have developed a three-component intermolecular trifluoromethylazolation of alkenes to deliver various trifluoromethylated azole derivatives. The method features exclusive chemo- and regioselectivity, a broad scope of alkenes and oxazoles, thiazoles, and good tolerance of functional groups under mild conditions. Preliminary mechanistic studies support a radical process for the transformation.

Synthesis of rare-earth metal complexes with a morpholine-functionalized ß-diketiminato ligand and their catalytic activities towards C-O and C-N bond formation.

Unusual tridentate ß-diketiminato rare-earth metal chlorides LRECl(µ-Cl)2Li(THF)2 (RE = Y (1a), Yb (1b), and Lu (1c); L = MeC(NDipp)CHC(Me)N(CH2)2NC4H8O; Dipp = 2,6-iPr2C6H3) and the corresponding dialkyl complexes LRE(CH2SiMe3)2 (RE = Y (2a), Yb (2b), and Lu (2c)) were prepared by reaction of a morpholine-functionalized ß-diketiminato proligand HL with anhydrous RECl3 and rare-earth metal trialkyl complexes RE(CH2SiMe3)3(THF)2, respectively. In 1 and 2, the morpholine moiety displayed a stable chair conformation and the resulting ligand coordinated to the rare-earth metal ion in a [NNN]-tridentate chelating fashion. Further studies demonstrated that these dialkyl complexes showed high activity towards the catalytic formation of C-O and C-N bonds in the alcoholysis of isothiocyanates and aminolysis of epoxides. A series of O-thiocarbamate derivatives were achieved in good to excellent yields by reaction of various alcohols with aromatic and aliphatic-substituted isothiocyanates at room temperature. In addition, under solvent-free conditions, the ring-opening reaction of terminal and internal epoxides with arylamines yielded the corresponding ß-amino alcohols with excellent regioselectivity. More importantly, a novel ß-diketiminato/anilido yttrium alkyl complex LY(NHDipp)(CH2SiMe3) (5a) was isolated and characterized by the stoichiometric reaction of 2a with diisopropylaniline.

Phosphinoamido ligand supported heterobimetallic rare-earth metal-palladium complexes: versatile structures and redox reactivities.

Heterobimetallic Ln(III)-Pd(0) complexes (Ln = Y, Sm, Gd, Yb) featuring tetranuclear structures with COD as bridges were obtained via the metallation of tris(phosphinoamido) rare-earth metal complexes [Ph2PNAd]3Ln (Ad = adamantyl) with (COD)Pd(CH2SiMe3)2. Notably, the Sc(III)-Pd(0) complex possesses a C3-symmetry with a very short Sc-Pd bond length of 2.432(2) Å, while the tetranuclear complexes exhibited versatile structures both in solution and in the solid state. Reduction of the trivalent complex (Ph2PNAd)3Yb with one equivalent of KC8 in the presence of 18-c-6 afforded the divalent complex [(Ph2PNAd)3Yb][(18-c-6)K(THF)2], which was further reacted with (Ph3P)4Pd to form the first Yb(II)-Pd(0) complex. The Pd(0) → Yb dative interaction weakened significantly from Yb(III) to Yb(II) based on computational studies, which was attributed to the attenuated Lewis acidity of the Yb(II) center. Reactions of Ln(III)-Pd(0) complexes (Ln = Sc and Yb) with the disulfide PhSSPh showed that the Pd(0) center served as a two-electron donor while the reaction apparently occurred on the Ln(III) centers to form Ln(III)-Pd(0) bis-sulfide complexes.

Rare-Earth-Metal-Complex-Catalyzed Hydroalkoxylation and Tandem Hydroalkoxylation/Cyclohydroamination of Isocyanates: Synthesis of Carbamates and Oxazolidinones.

Novel N,N,N-tridentate ß-diketiminato rare-earth-metal dialkyl complexes LRE(CH2SiMe3)2 [RE = Y (1a), Gd (1b), Yb (1c), Lu (1d); L = MeC(NDipp)CHC(Me)N(CH2)2NC4H8, where Dipp = 2,6-iPr2C6H3] have been conveniently synthesized by one step from reactions of the rare-earth-metal trialkyl complexes RE(CH2SiMe3)3(THF)2 (THF = tetrahydrofuran) with a pyrrolidine-functionalized ß-diketiminate HL, and their catalytic behaviors toward hydroalkoxylation and tandem hydroalkoxylation/cyclohydroamination of isocyanates have been described. These rare-earth-metal catalysts exhibited high efficiency in the hydroalkoxylation of isocyanates, providing a variety of N-alkyl and N-aryl carbamate derivatives under mild reaction conditions with a rather low catalyst loading (0.04 mol %). More significantly, they can promote a tandem hydroalkoxylation/cyclohydroamination reaction between terminal and internal propargylic alcohols with substituted arylisocyanates, leading to the efficient synthesis of methylene and (Z)-selective arylidene oxazolidinones in good-to-high yields via consecutive C-O and C-N bond formation. The stoichiometric reaction of 1a with p-tolylisocyanate generated an unusual dinuclear yttrium complex, {[η2-(4-MePhNCO)(CH2SiMe3)]Y[µ-η2:η1:η1-(4-MePhNCO)CC(Me)(NDipp)C(Me)N(CH2)2NC4H8]}2 (7a), with two different amidate units, which underwent an sp2 C-H bond activation of the ß-diketiminato backbone, followed by the insertion of isocyanate.

Synthesis and characterization of rare-earth metallate amido complexes bearing the 2-amidate-functionalized indolyl ligand and their application in the hydroboration of esters with pinacolborane.

The reactions of 2-amidate-functionalized indolyl proligand 2-(2,6-iPr2C6H3NHCO)C8H5NH (H2L) with [(Me3Si)2N]3RE(µ-Cl)Li(THF)3 were studied leading to the synthesis and characterization of a series of novel discrete trinuclear rare-earth metallate amido complexes containing the anion [{η1:(µ2-η1:η1):η1-LREN(SiMe3)2}3(µ3-Cl)]- and cation Li+(THF)4 (RE = Y(1a), Nd (1b), Sm (1c), Gd (1d), Dy (1e), Er (1f), and Yb (1g)) in good yields by silylamine elimination. All of the complexes were characterized by spectroscopic methods, elemental analyses and single-crystal X-ray diffraction, and complexes 1a and 1c were additionally characterized by NMR spectroscopy. As proof of principle of their activity, these complexes were used as precatalysts for the hydroboration of esters using HBpin as the hydride source displaying high activity under neat and room temperature conditions. As a result, the ligand, ionic and multinuclear cooperative effects on catalytic activity were observed.

Transformation of the sp2 Carbanion to Carbene with Subsequent 1,1-Migratory Insertion and Nucleophilic Substitution in Rare-Earth Metal Chemistry.

The development of Fischer-type electrophilic carbene chemistry with early transition metals has been a great challenge due to the fact that such metals in their high oxidation states lack the d electrons to stabilize the electrophilic carbene. Herein, we disclose the first experimental and theoretical findings of in situ transformation of an sp2 carbanion to a Fischer-type electrophilic carbene with rare-earth metals in their high oxidation state with a d0 electron via electron transfer. The carbene may undergo 1,1-migratory insertion into an adjacent RE-C(sp3) bond, and an unprecedented ring opening of the indole ring of the ligand occurs when the carbenes undergo nucleophilic substitution with a special organolithium reagent o-Me2NC6H4CH2Li. The key to success is the uniquely tailored novel ligand systems featuring a suitable conjugate building block (-C═C-C═N) bearing an sp2 carbanion connected to the rare-earth metal center.

Three-Coordinate Pd(0) with Rare-Earth Metalloligands: Synergetic CO Activation and Double P-C Bond Cleavage-Formation Reactions.

Metalation of ß-diketiminato rare-earth metal complexes LnacnacLn(PhNCH2PPh2)2 (Ln = Y, Yb, Lu) with (COD)Pd(CH2SiMe3)2 afforded three-coordinate Pd(0) complexes supported by two sterically less bulky phosphines and a Pd → Ln dative interaction. The Pd(0) center is prone to ligation with isonitrile and CO; in the latter case, the insertion of a second CO with the Y-N bond was assisted via a precoordination of CO on the Pd(0) center, which led to the formation of an anionic Pd(0) carbamoyl. The reaction of the Pd-Y complex with iodobenzene showed a remarkable double P-C bond cleavage-formation pathway within the heterobimetallic Pd-Y core to afford (Ph3P)2PdI(Ph), imine PhNCH2, and a ß-diketiminato yttrium diiodide. In the related reaction of LnacnacY(PhNCH2PPh2)2 with (Ph3P)2PdI(Ph), the P-C bond cleavage following with a N-C bond formation was observed. Computational studies revealed a synergetic bimetallic mechanism for these reactions.

Dehydrogenative Coupling of Terminal Alkynes with O/N-Based Monohydrosilanes Catalyzed by Rare-Earth Metal Complexes.

Newly synthesized rare-earth metal alkyl complexes bearing a tripyrrolyl ligand act as excellent precatalysts for the cross-dehydrogenative coupling between various terminal alkynes and O/N-based monohydrosilanes of HSi(OEt)3/HSi(NMe2)3, leading to the formation of a variety of alkoxysilylalkyne and aminosilylalkyne derivatives in good to high yields. The precatalysts LRE(CH2SiMe3)(thf)2 (RE = Y(1a), Er(1b), Yb(1c), L = 2,5-[(2-C4H3N)CPh2]2(C4H2NMe), thf = tetrahydrofuran) were easily prepared in high yields via the reactions of RE(CH2SiMe3)3(thf)2 with the proligand H2L in a single step. Mechanistic studies reveal that treatment of 1 with phenylacetylene could generate the active catalytic species: dinuclear rare-earth metal alkynides (L(thf)n[RE(µ-C≡CPh)]2L) (RE = Y(5a), n = 1; Yb(5c), n = 0), which could react with HSi(OEt)3 to produce the coupling product 4aa and the dinuclear rare-earth metal hydrides (L (thf)[RE(µ-H)]2L) (RE = Y(6a); Yb(6c)). By contrast, prior treatment of 1c with HSi(OEt)3 proceeds via cleavage of the Si-O bond to produce the dinuclear ytterbium alkoxide (LYb(µ-OEt))2 7c, which is inert in the dehydrogenative coupling reaction. The results of the mechanistic studies are consistent with the observation that the reaction is greatly influenced by the addition sequence of precatalyst/alkynes/silanes.

Heterobimetallic Pd(0) complexes with Pd→Ln (Ln = Sc, Y, Yb, Lu) dative bonds: rare-earth metal-dominated frustrated Lewis pair-like reactivity.

A series of heterobimetallic Pd-Ln complexes with Pd→Ln (Ln = Sc, Y, Yb, Lu) dative bonds were synthesized via sequential reactions of phosphinoamine Ph2PNHAd with (Me3SiCH2)3Ln(THF)2 and (Ph3P)4Pd or (COD)Pd(CH2SiMe3)2. These complexes were characterized by NMR spectroscopy, X-ray diffractions, and computational as well as electrochemical studies, which revealed Pd→Ln dative interactions that vary according to the ionic radii of Ln3+. Furthermore, the notable dynamic structural features of the Pd-Ln complexes in solution and their unexpected frustrated Lewis pair-like reactivity toward aryl halides and ketene were also studied.

Syntheses of Dianionic α-Iminopyridine Rare-Earth Metal Complexes and Their Catalytic Acitivities toward Dehydrogenative Coupling of Amines with Hydrosilanes.

Reactions of [(Me3Si)2N]3RE(µ-Cl)Li(THF)3 with aminomethylene-substituted pyridine 2-[O(CH2CH2)2NCH2CH2NCH2]C5H4N (1) gave the dianionic α-iminopyridine rare-earth metal amido complexes {µ-η2:σ1:κ1:κ1-2-[O(CH2CH2)2NCH2CH2NCH]C5H4N}2RE2[N(SiMe3)2]2 (RE = Y(2a), La(2b), Pr(2c), Nd(2d), Sm(2e), Dy(2f), Er(2g), and Lu (2h)). However, reaction of [(Me3Si)2N]3Y(µ-Cl)Li(THF)3 with pyridin-2-ylmethyl-substituted amines such as 2-(RNHCH2)C5H4N (R = tBu (3a) and 2,6-iPr2Ph (3b)) or benzyl-substituted amine O(CH2CH2)2NCH2CH2NHCH2C6H5 (5) afforded the corresponding yttrium complexes containing monoanionic ligands [2-(RNCH2)C5H4N]2YN(SiMe3)2 (R = tBu (4a) and 2,6-iPr2Ph (4b)) or [O(CH2CH2)2NCH2CH2NCH2C6H5][(Me3Si)2N)]Y(µ-Cl)(µ-η3-O(CH2CH2)2NCH2CH2NCH2C6H5)Li(THF) (6). Dianionic α-iminopyridine rare-earth metal amido complexes showed high catalytic activities for the dehydrogenation coupling reaction of hydrosilanes and amines providing a variety of silylamines in high yields.

Heterobimetallic scandium-group 10 metal complexes with LM → Sc (LM = Ni, Pd, Pt) dative bonds.

Heterobimetallic scandium complexes with whole group 10 metals were synthesized. All Sc-LM complexes were characterized by NMR spectroscopy, X-ray diffraction analysis and computational studies, which revealed notable LM → Sc (LM = Ni, Pd, Pt) dative bonding interactions in these heterobimetallic systems. Versatile coordination modes toward apical donors were observed in these heterobimetallic Sc-LM complexes, among which the Sc-Ni complexes 2 and 3 were reversibly bound to N2 and the Sc-Pt complex 5 was coordinated to an additional PPh3 ligand, while in the Sc-Pd complex 4 no apical donor was ligated.

Aluminum complexes with Schiff base bridged bis(indolyl) ligands: synthesis, structure, and catalytic activity for polymerization of rac-lactide.

A series of Schiff base bridged bis(indolyl) ligands were developed for aluminum chemistry. The reactions of AlEt3 or AlMe3 with the Schiff base bridged bis(indolyl) proligands R1(-N[double bond, length as m-dash]CHC8H5NH)2 (R1 = -CH2CH2- (H2L1); -CH2CH2CH2- (H2L2); -CH2CMe2CH2- (H2L3); rac-Cy (H2L4); and R,R-Cy (H2L5)) were studied leading to the synthesis of a series of aluminum alkyl complexes L1AlEt (1)-L5AlEt (5) and L3AlMe (3b) in good yields, while the reaction of H2L3 with Al(OiPr)3 gave the aluminum alkoxide complex L3AlOiPr (3a). These aluminum complexes were characterized by spectroscopic methods and elemental analyses. The solid state structures of the aluminum complexes 1-5 and 3a were confirmed by the X-ray diffraction study. X-ray analyses revealed that the aluminum centre in these complexes is five-coordinated. The coordination geometry is between square pyramidal and trigonal bipyramidal. In the presence of 1 equiv. of isopropanol, the aluminum alkyl complexes exhibited notable activity towards the ring-opening polymerization of rac-lactide at 70 °C in toluene, with good control over molecular weights and dispersities. The substituents and the length of the bridging part between the two Schiff base nitrogen atoms have an influence on either the tacticity of isolated polymers or the rate of polymerization. The kinetics of complex L3AlOiPr (3a) in C6D6 was also investigated, and the experimental results revealed that the rate of polymerization was first-order with respect to rac-lactide.

Copper Salts/TBAB-Catalyzed Chemo- and Regioselective ß-C(sp3)-H Acyloxylation of Aliphatic Amides.

An efficient Cu(II)-catalyzed and tetrabutylammonium bromide (TBAB)-promoted strategy for highly regioselective and chemoselective C(sp3)-H acyloxylation of aliphatic amides is described. Acyloxylation occurs selectively at the ß position with a broad substrate scope of carboxylic acids and aliphatic amides and good functional group compatibility. Notably, the competing reaction of intramolecular dehydrogenative amidation and intermolecular acyloxylation could be efficiently controlled by the amount of copper salt and the addition of TBAB. The intramolecular dehydrogenative amidation product was obtained in high yield when the amount of copper salts was increased. However, when TBAB was used as an additive, a preference for acyloxylation over intramolecular amidation was observed and the acyloxylated products were obtained in good yield. Preliminary studies were carried out to gain insights into the mechanism.

Synthesis and characterization of 2-t-butylimino-functionalized indolyl rare-earth metal amido complexes for the catalytic addition of terminal alkynes to carbodiimides: the dimeric complexes with the alkynide species in the µ-η1:η2 bonding modes.

A series of new rare-earth metal amido complexes bearing a 2-t-butylimino-functionalized indolyl ligand were synthesized via dehydrogenation of a secondary amine, and their reactivities and catalytic performances were investigated. The reactions of 2-(tBuNHCH2)C8H5NH (1) with rare-earth metal amides [(Me3Si)2N]3RE(µ-Cl)Li(THF)3 afforded the complexes [2-(tBuN[double bond, length as m-dash]CH)C8H5N]RE[N(SiMe3)2]2 (RE = Er (2), Y (3), Dy (4), Sm (5), Nd (6)) containing the bidentate ligand via dehydrogenation of the amine to the imine group. Complexes 2-6 exhibited an excellent catalytic activity for the addition of terminal alkynes to carbodiimides affording a series of corresponding N,N'-dialkyl-propiolamidines. The catalysts can also be efficiently used for the preparation of the sterically bulky N,N'-diaryl-propiolamidine. Furthermore, the dimeric complexes {(µ-η1:η2-RC[triple bond, length as m-dash]C)RE[2-(tBuN[double bond, length as m-dash]CH)C8H5N]2}2 (11: RE = Y, R = Ph; 12: RE = Yb, R = SiMe3), with the alkynyl ligand in the µ-η1:η2 haptic modes, were isolated in attempts to study the catalytic mechanism.

A Scandium Metalloligand-Based Heterobimetallic Pd-Sc Complex: Electronic Tuning Through a Very Short Pd→Sc Dative Bond.

The first heterobimetallic Pd-Sc complex featuring a very short Pd→Sc dative bond has been synthesized and characterized by multinuclear NMR spectroscopy, X-ray diffraction analysis, and electrochemistry. Computational studies elucidated the nature of the Pd→Sc bond as a donor-acceptor interaction, which generates a more electron-deficient Pd0 metal center as compared to that in the mono Pd0 complex in their reactions with isonitrile and carbon monoxide. Cooperative reactivity has been demonstrated in the reaction with MeI.

Synthesis, characterization, and reactivity of dinuclear organo-rare-earth-metal alkyl complexes supported by 2-amidate-functionalized indolyl ligands: substituent effects on coordination and reactivity.

Two series of new dinuclear organo-rare-earth-metal alkyl complexes supported by 2-amidate-functionalized indolyl ligands with different haptic modes were synthesized and characterized. The treatment of [RE(CH2SiMe3)3(THF)2] with 1 equiv. of 2-(2,6-iPr2C6H3NHC[double bond, length as m-dash]O)C8H5NH (H2L1) and 2-(2-tBuC6H4NHC[double bond, length as m-dash]O)C8H5NH (H2L2) in toluene yielded the dinuclear organo-rare-earth-metal alkyl complexes {[η1:(µ2-η1:η1)-L1]RE(CH2SiMe3)(THF)2}2 [RE = Gd (1a), Dy (1b), Y (1c), Er (1d), and Yb (1e)] and {[η1:(µ2-η1:η1):η1-L2]RE(CH2SiMe3)(THF)2}2 [RE = Gd (2a), Dy (2b), Y (2c), Er (2d), and Yb (2e)] in good yields. When [RE(CH2SiMe3)3(THF)2] were treated with 2 equiv. of H2L1 or H2L2 in THF, the dinuclear organo-rare-earth-metal complexes {(η1:η1-HL)[η1:(µ2-η1:η1):η1-L]RE(THF)}2 (1ca: RE = Y, L = L1; 2ea: RE = Yb, L = L2) were obtained. The complexes could react with small organic molecules such as N,N'-diisopropylcarbodiimide (DIC), phenyl isocyanate, N-methylallylamine, phenylacetylene, pyridine, N-phenylimidazole, or 4-dimethylaminopyridine (DMAP) to yield a series of new complexes with different reactivity patterns along with the reported rare-earth-metal alkyl complexes. In the presence of cocatalysts, these dinuclear organo-rare-earth-metal alkyl complexes could initiate isoprene polymerization with high activity (100% conversion of 2000 equiv. of isoprene in 12 h), yielding polymers with high regioselectivity (1,4 polymers up to 96.1%).