31P CP MAS NMR Research Articles

Mechanistic Insights into the Appel Reaction Mediated by a Poly-Phosphamide Material as a Heterogeneous Catalyst.

Due to notable thermochemical stability, polyphosphamides are often regarded as flame retardants, while molecular phosphamides can serve as versatile Lewis base to catalyze diverse organic transformations. Being chemically analogous to phosphine oxide, phosphamide can also be considered as a mediator for the phosphine-mediated reaction. Herein, an amorphous polymeric material consisting of phosphamide (-NH-P(O)) in the repeating unit (POP) has been prepared via condensation of tris(2-aminoethyl)amine (TREN) and phenyl phosphinic dichloride (PPDC). The POP is isolated as a metal-free and pure organic material which is made of a strong covalent bond and the phosphamide unit is deployed in the organic framework. The presence of phosphamide in the repeating unit of the isolated amorphous POP material can be confirmed by 31P CPMAS NMR, FTIR, and Raman studies. The core-level N 2p and P 2p X-ray photoelectron spectra are in accordance with the presence of tertiary amine nitrogen attached to carbon and secondary amine nitrogen attached to phosphorus. Elemental analyses have depicted approximately 19.7% of phosphorus content in the material, which is being utilized to study the catalytic Appel reaction with 76% conversion of alcohol to a corresponding halide and TON of 462. Quasi in situ Raman study has identified that amino phosphine formed via in situ reduction of the phosphamide unit of the POP catalyzes the halogenation of primary and secondary alcohols with wide substrate scope and functional group tolerance. Kinetic studies have established a first-order dependence with respect to alcohol, while deuterium labeling experiments emphasize that the deprotonation of alcohol is the rate-limiting step. High thermal stability of the material, scope of easy catalyst recyclability, and a cumulative TON of 1386 have led the POP as an emerging pure organic material to be explored further for other phosphine-mediated organocatalysis.

Unveiling the mechanistic aspects of methylene blue adsorption onto a novel phosphate-decorated coconut fiber lignin

The aim of this work was to evaluate the adsorptive performance of the phosphorylated coconut fiber lignin (PCFL) obtained through an innovative biorefinery process for removing methylene blue (MB). PCFL was obtained using coconut fiber mixed with 85 % wt. H3PO4 at 70 °C for 1 h. Milled wood lignin (MWL) and PCFL were characterized by FTIR, CP-MAS 31P NMR, phosphorous and hydroxyl contents, pHPZC, and BET analyses. The batch adsorption tests evaluated the effects of the biosorbent (0.25 – 4 g L-1) and adsorbate dosages (2.5 – 7.5 mg L-1), contact time (0 – 60 min), pH (4 – 8), ionic strength (0.001 – 0.1 mol L-1) and temperature (298.15 – 318.15 K) on MB adsorption. Kinetic, equilibrium, and thermodynamic modeling were used. The phosphorous content on PCFL was 2.5 times higher than that of MWL. PCFL presented an enhanced adsorptive performance for removing MB, which was spontaneous (ΔG0 < 0), endothermic (ΔH0 > 0), with affinity between the biosorbent and adsorbate (ΔS0 > 0), and driven by physisorption (Ea > 40 kJ mol-1). The adsorptive performance of PCFL was enhanced due to the grafting of new active sites by using an innovative biorefinery process, showing its potential to be used for textile effluent remediation.

Hypophosphite cross-linked starch succinate/chitosan membranes as alternative for packaging and pharmaceutical application

The growing industrial demand for valuable biomaterials contributes to modifying readily available starch to give it the desired functional properties. The advantage of the reported studies was the modification of starch with succinic acid via sodium hypophosphite as a cross-linker. The cross-linked structure was confirmed with Raman, ATR-FTIR, 13C and 31P CP-MAS NMR spectroscopies. In the next step, the phosphonated starch succinate/chitosan materials were prepared for application in food packaging and coatings. The most desirable features for such employment were achieved, such as a low water vapour permeability through the membranes (~2 %) and accelerated biodegradability compared to starch film attributes. Significant differences in these properties resulting from the time of synthesis and the quantitative composition of the films were verified. The longer synthesis time of composites affected the better mechanical properties (Elongation at break, εb =~91–94 %, and Young's Modulus, E = 140‐160 MPa). Thermal parameters (including FTIR analysis of gaseous products evolved during the thermal decomposition) were confirmed. The changes in ordering behaviour (crystallinity degree, Xc) determined with XRD varied from 23 % (for the starch film) to 10–21 % (starch in composites). Obtained biodegradable starch-based materials may constitute an attractive ecological alternative for plastics.

Bioactive nanoglasses and xerogels (SiO2–CaO and SiO2–CaO–P2O5) as promising candidates for biomedical applications

A binary and ternary system of highly bioactive nanoparticles of xerogel (88SiO2–12CaO (wt.%), solvXG88, 78SiO2–16CaO–6P2O5, solvXG78P6) and glass (69SiO2–25CaO–6P2O5, solvBG69P6) were prepared following an unconventional solvothermal path of the synthesis. These nanosized (<50 nm), non-spherical in shape and mesoporous materials with different compositions greatly enhanced the formation process of hydroxyapatite (HA) in simulated physiological fluids compared to reference 45S5 glass, commonly used in orthopedics and dentistry. The deposition of a HA layer on the glasses was analyzed by various techniques, namely XRD, IR-ATR, 31P CP-MAS NMR, EDS analyses, SEM, and HR-TEM imaging. For both types of nanoparticles (glass and obtained at lower temperature xerogels) superior apatite-mineralization ability in time as short as 4 h in the physiological-like buffer was achieved thus, exceeded the bioactivity of the 45S5 glass. This unique bioactivity was complemented by biocompatibility with human dermal fibroblasts and MC3T3 mouse osteoblast precursors, verified in a wide range of concentrations, as well as hemocompatibility studies. The most promising candidate which can compete with clinically used Bioglass is solvXG78P6.

Silica Nanopowder Supported Frustrated Lewis Pairs for CO2 Capture and Conversion to Formic Acid.

Treatment of hydroxylated silica nanopowders S1 and allyl-functionalized silica nanopowders S2 with 3-(diphenylborano)- or 3-bis(pentafluorophenylborano)propyltrimethoxysilane or 2-(diphenylphosphino)- or 2-(dicyclohexylphosphino)ethyltriethoxysilane generates silica nanopowder supported Lewis acids S3 and silica nanopowder supported Lewis bases S4. These surfaces were characterized by 13C, 11B, and 31P cross-polarization magic angle spinning nuclear magnetic resonance (CP MAS NMR), X-ray photoelectron spectroscopy (XPS), and attenuated total reflection Fourier transform infrared (ATR FTIR). When S3 is combined with solution-phase Lewis bases PR3 (R = C6F5, C6H5, mesityl), six associated silica nanopowder supported frustrated Lewis pairs (FLPs) are formed. In another set of six reactions, the interactions between the supported Lewis bases S4 and solution-phase Lewis acids BR3 with R = C6F5, C6H5, mesityl produced six more associated supported FLPs. The capture of CO2 by these FLPs producing FLP-CO2 Lewis pair adducts S5 and S6 were highlighted by ATR FTIR, and it was found that FLP S5e with R = C6H5 on both the supported Lewis acid and solution-phase Lewis base trapped the largest quantities of CO2 on the silica nanopowder supports. Conversion of CO2 to HCOOH was achieved by first activating H2 to generate activated FLP-H2 surfaces S7 and S9. Addition of CO2 then generated HCOOH via the silica nanopowder supported FLP-HCOOH adducts S8 and S10. Qualitative identification of HCOOH generation was achieved by ATR FTIR measurements, and surface 10b with R = C6H5 proved to be the most successful silica nanopowder surface bound FLP in HCOOH generation. In some cases, diborano formates (-BO(CH)OB-) S11 and S12 were also identified as side products during HCOOH formation. Spectroscopic characterization of purposefully synthesized S11 and S12 included 11B and 31P CP MAS NMR.

Solid-State NMR, X-Ray Diffraction, and Theoretical Studies of Neutral Mononuclear Molecular Bis(triphenylphosphine)silver(I) Mono-Carboxylate and -Nitrate Systems

Neutral mononuclear molecular silver(i) carboxylate complexes of the form [(Ph3P)2Ag(O2XY)] with O2XY=O2CCH2Ph, O2CCHPh2, O2CC(CH3)3, O2CCH2C(CH3)3, and O2CCF3 (compounds 1–4 and 5β) have been investigated in the solid state using single-crystal X-ray structure determinations, 1D 31P CPMAS NMR and 2D 31P–31P CPCOSY NMR measurements, and ab initio computational modelling. The results show that these complexes contain P2AgO2 molecular cores with four-coordinate silver in which the carboxylate ligands are weakly bound to the silver atoms via the two oxygen atoms giving rise to unsymmetrical chelate units. Crystal structure determinations and solid-state NMR spectra have also been analysed for the mononuclear molecular silver(i) nitrate complex [(Ph3P)2Ag(O2NO)] (9α) and two polymorphs of its toluene monosolvate (11α, β). In 9α, the two PPh3 ligands are of the same chirality, whereas in 11α, β, they are opposed. The crystalline environments in the polymorphs have been explored by way of Hirshfeld surface analyses, after quantum-mechanical isolated-molecule calculations had shown that although the molecular energies of the experimental geometries of 9α, and 11α, β are significantly different from each other and from the energies of the optimized geometries, the latter, in contrast, do not differ significantly from each other despite the conformational isomerism. It has further been shown using 9α as an example that the energy dependence on variation of the P–Ag–P angle over a range of ~15° is only ~5 kJ mol−1. All this indicates that the forces arising from crystal packing result in significant perturbations in the experimental geometries, but do not alter the stereoisomerism caused by the donor atom array around the Ag atom. In the NMR study, a strong inverse correlation has been found between 1J(107/109Ag,31P) and the Ag–P bond length across all carboxylate and nitrate compounds.

Selective uptake of La3+ ions with polyoxometalates-functionalized mesoporous SBA-15: An EXAFS study

Abstract In this work, mesoporous materials based on inorganic/organic polyoxometalate (POMs) hybrids with the ability of further incorporating heterometallic lanthanum cations were designed. On the basis of the La3+ coordination to vacant organophosphonyle derivatives of POMs previously studied, herein POMs-grafted onto an amino-functionalized mesoporous SBA-15 ({NH2}-SBA-15) with incorporated La3+ ions were synthesized by varying the amounts of the latter. LIII-edge La EXAFS spectroscopy of the resulting materials provided local structural information around LaIII ions (i.e. number, nature and distances of neighboring atoms), which are comparable to that of the LaIII complexes of POMs hybrids. This technique, in addition with 31P CP-MAS NMR spectroscopy, gave definitive clues for a selective uptake of the incorporated La3+ ions by the POMs grafted onto the {NH2}-SBA-15 supports. This study is a clear demonstration that, due to their chelate effect, POMs hybrids act as efficient ligands for La3+ even in the presence of competitive adsorption sites. Consequently, a regular distribution of the La3+ ions along the channels of the SBA-15 is thus observed in these materials due to the nanostructuration of the POMs onto the support.

Immobilization of polyoxometalate hybrid catalysts onto mesoporous silica supports using phenylene diisothiocyanate as a cross-linking agent

Abstract The hybrid derivative of heteropolytungstate bearing two aniline groups, namely (nBu4N)3[NaHPW9O34{As(O)C6H4NH2}2], was post-functionalized in the presence of 1,4-phenylene diisothiocyanate (PDITC). The resulting molecular moiety was characterized by IR, 1H and 31P NMR spectroscopy. In a second step, this post-functionalized hybrid of polyoxometalate was covalently grafted onto the surface of an amino-functionalized SBA-15 silica by means of the formation of thiourea bonds. This simple and efficient strategy of immobilization did not require the use of a coupling agent and was performed in mild reaction conditions. Various physicochemical techniques (13C and 31P CP MAS NMR spectroscopies, XPS, XRF, HR-TEM microscopy and N2 sorption) contributed to the full characterization of the supported catalyst. In addition HR-TEM was found to be an essential technique for the identification of the polyoxometalate units inside the pores of SBA-15. Finally, the catalytic performances of the supported polyoxometalates were evaluated in the epoxidation of cyclooctene with aqueous H2O2 in acetonitrile at 50 °C.

Preparation of phosphotungstic acid based poly(ionic liquid) and its application to esterification of palmitic acid

Abstract For biodiesel production from waste cooking oils with high acid values, an inefficient esterification pretreatment is always conducted to convert free fatty acids (FFAs) before alkali-catalysed transesterification process. In this paper, phosphotungstic acid based poly(ionic liquid) was prepared to catalyse the esterification of palmitic acid with methanol while the required catalyst dosage was much lower than commercial Amberlyst-15. And the catalyst was characterized by 31P CP-MAS NMR, FTIR, SEM, XRF and TG. Among the three poly(ionic liquid)s prepared in this paper, phosphotungstic acid based poly(ionic liquid) was selected to be the most suitable catalyst for esterification because the catalyst could be reused for more than 5 times without significant deactivation. According to single factor analyses, the esterification yield could reach 91.6% after 8 h while the reaction temperature, methanol to acid molar ratio and catalyst dosage were 65 °C, 6 and 3% wt, respectively. Afterwards, palmitic acid was proposed to be first adsorbed on the catalyst before reacting with methanol. Finally, a palmitic acid adsorbed Eley-Rideal model was employed to analyse the reaction and the adsorption mechanism was assumed as well.

Interfacial Behavior of Orthoborate Ionic Liquids at Inorganic Oxide Surfaces Probed by NMR, IR, and Raman Spectroscopy

Absorption modes and the reactivity of nonhalogenated ionic liquids (ILs) at inorganic oxide surfaces of γ-Al2O3, MgO, and SiO2 particles were characterized using multinuclear (11B, 31P, and 29Si) solid-state magic-angle-spinning NMR, FTIR, and Raman spectroscopy. ILs are composed of the trihexyl(tetradecyl)phosphonium cation, [P6,6,6,14]+, and bis(mandelato)borate, [BMB]−, or bis(salicylato)borate, [BScB]−, anions. Spectroscopic measurements were performed on room-temperature (298 K) samples and samples exposed to 15 h at 373 K. The single-pulse 11B NMR data of heated [P6,6,6,14][BMB] mixed with the inorganic oxides showed a significant change in the spectra of the anion for all three oxides. In contrast, no such spectral changes were detected for heated [P6,6,6,14][BScB] mixed with the inorganic oxides. 31P MAS NMR data for the IL/metal oxide systems revealed interactions between [P6,6,6,14]+ and the surfaces of oxides. A significant intensity of 31P CP-MAS NMR signals indicated a low mobility of cation...

Performance and mechanisms of emerging animal-derived biochars for immobilization of heavy metals

Animal-derived biochars (ADBs) are a series of newly emerging biochars from the pyrolysis of animal carcasses. Their elemental composition and structural properties would be quite different to those of plant-based biochars and/or manure-derived biochars (MDBs). In this work, ADBs derived from cattle and swine carcasses were applied to investigate their sorption potentials and mechanisms for immobilization of Pb(II), Cd(II), Cu(II), and Hg(II). ADBs showed high calcium (Ca; >27%) and phosphorus (P; >15%) contents and relatively low carbon (C; <8%) content. Ca and P were present in the skeleton as calcium–phosphate complexes, dominantly as hydroxyapatite (HAP), which was identified by CP–MAS 31P NMR analysis. By contrast, the reference biochars derived from cattle, swine, and poultry manures possessed low Ca (<13%) and P (<4%) contents and relatively high C (>30%) content. Sorption experiments showed that ADBs were more effective in immobilizing Pb(II), Cd(II), and Cu(II) than MDBs. However, the affinities of ADBs for Hg(II) were lower than those of MDBs. Characterization analyses indicated that Pb(II) was effectively immobilized via precipitation, whereas ion exchange was the dominant mechanism in combining Cd(II) or Cu(II) with ADBs. ADBs are unsuitable for immobilizing Hg(II) because of the lack of oxygen-containing functional groups on the C surface, which can induce the reduction of Hg(II) to form Hg2Cl2. The immobilized heavy metals were difficult to be rereleased from ADBs in simulated acid rain environment. Hence, ADBs are promising biochars for immobilizing Pb(II), Cd(II), and Cu(II).

WITHDRAWN: An example of S,S′-bidentate coordination mode of the dithiophosphate group in the heteroleptic tetraphenylantimony(V) complex, [Sb(C6H5)4{S2P(O-cyclo-C6H11)2}]: Multinuclear (13C, 31P) CP MAS NMR, single-crystal X-ray diffraction studies and thermal behaviour

Crystalline O,O′-di-cyclo-hexyl dithiophosphate (Dtph) tetraphenylantimony(V) complex, [Sb(C6H5)4{S2P(O-cyclo-C6H11)2}] (1) was prepared and studied by means of heteronuclear (31C, 31P) CP MAS NMR ...

31P-Solid-State NMR Characterization and Catalytic Hydrogenation Tests of Novel heterogenized Iridium-Catalysts

The synthesis of novel robust and stable iridium-based immobilized catalysts on silica-polymer hybrid materials (Si-PB-Ir) is described. These catalysts are characterized by a combination of ¹D ³¹P CP-MAS and 2D ³¹P-¹H HETCOR and J-resolved multinuclear solid state NMR experiments. Different binding situations such as singly and multiply coordinated phosphines are identified. Density functional theory (DFT) calculations are performed to corroborate the interpretation of the experimental NMR data, in order to propose a structural model of the heterogenized catalysts. Finally, the catalytic activity of the Si-PB-Ir catalysts is investigated for the hydrogenation of styrene employing para-enriched hydrogen gas.

Direct Synthesis of Low-Coordinate Pd Catalysts Supported on SiO2 via Surface Organometallic Chemistry

Highly dispersed low-coordinate Pd sites on SiO2 are fabricated by grafting the PdII PCP-pincer complex (tBuPCP)Pd–OH (tBuPCP = 2,6-C6H3(CH2PtBu2)2) on SiO2, followed by calcination with ozone (100 °C) and reduction with H2 (300 °C). The chemisorption process and structure of this organometallic complex on SiO2 is established by solution-phase 1H and 31P NMR and solid-state 31P CPMAS NMR spectroscopy, XPS, DRIFTS, and AC-HAADF-STEM. The CO adsorption properties of the Pd centers reveal a surprisingly high fraction of adsorption sites where CO is bound in a linear fashion, indicative of low-coordinate Pd. Furthermore, enhanced selectivity of these catalyst centers in aerobic alcohol oxidation versus a control catalyst argues that these low-coordinate sites are the catalytically active sites.

A methods study of immobilization of PONOP pincer transition metal complexes on silica polyamine composites (SPC)

Immobilization of catalytically active transition metal complexes on silica polyamine composite (SPC) surfaces offers many advantages for applications in catalysis particularly for catalyst recovery and reuse. We report here the immobilization of PONOP pincer complexes of Ru, Rh, Ni and Pd on the poly(allylamine) SPC, BP-1 using the Mannich reaction. Three different methods have been investigated for synthesizing the PONOP pincer transition metal complexes on BP-1: 1) direct reaction of the preformed pincer complexes using a two step Mannich reaction; 2) immobilization of the PONOP ligand using the Mannich reaction followed by the addition of a transition metal compound of a given metal; 3) the stepwise construction of PONOP on BP-1 followed by addition of a transition metal compound. The immobilized complexes on BP-1 were characterized by FT-IR, solid-state CPMAS 13C and 31P NMR, as well as elemental analysis. Anchoring of the complexes on BP-1 was also evaluated by the metal loading data obtained from the digestion of the loaded composites followed by Atomic Absorption Spectroscopy (AAS) or Inductively Coupled Plasma Atomic Emission Spectroscopy (ICPAES). The results showed that method 1 works better for the loading of pincer complexes on the SPC than methods 2 and 3. In the case of the Ru and Ni pincer complexes reasonable agreement with the phosphorous analysis was realized, while for the Pd complex values were high relative to the loading predicted from the phosphorus analysis, indicating the formation of the Pd nanoparticles on the surface during immobilization. For the Rh and Ru immobilized complexes with methods 2 & 3, metal loading was lower than the phosphorous analysis and this is attributed to entrained triphenylphosphine from the starting rhodium and ruthenium complexes based on the 13C and 31P CPMAS NMR data. Solution experiments using the PONOP pincer ligand and the Ru(PONOP) complex with n-butyl amine were conducted to model the site of electrophilic aromatic substitution on the pyridine ring. It was found that substitution both meta- and para-to the nitrogen takes place and this helped in the interpretation of the solid-state data.

Advanced NMR methodologies and micro-analytical techniques to investigate the stratigraphy and materials of 14th century Sienese wooden paintings

In this study a multi-analytical approach was used to characterize ancient and modern constitutive materials and the stratigraphy of a Sienese wooden painting consisting of four cusps belonging to a lost Polyptych, by Andrea di Bartolo dated back to the late 14th century, repainted in the 16th century and partially restored and cleaned in the 20th century. In order to distinguish the original layers from the other ones, a comparison with the painting Adorazione dei Magi by Bartolo di Fredi (Andrea's father) dated to the 14th century, was performed. The painting Adorazione dei Magi was found to be in a very good state of conservation and provided a model of the artistic technique used in Sienese painting in the 14th century.In situ measurements by portable NMR were performed to investigate the stratigraphy of the paintings in a non-destructive and non-invasive way. By means of this technique, information about all layers constituting the paintings were obtained and used to plan the successive micro-sampling. High resolution NMR spectroscopy was applied on a few samples to characterize binders and organic substances. Specifically, solid state 13C and 31P CPMAS NMR spectroscopy and 1H NMR spectroscopy in solution were applied to characterize original and non-original materials. Other techniques such as ToF-SIMS, HPLC, IR and Raman spectroscopy were also applied.

Synthesis and characterization of a new cyclohexaphosphate, (C6H7ClN)6P6O18·0.5(H2O)

A new cyclohexaphosphate with the composition (C6H7ClN)6P6O18·0.5(H2O) has been synthesized at room temperature in the presence of 4-chloroaniline as organic template and investigated by various physicochemical techniques. Its unit cell is triclinic P-1 with parameters a = 9.0054(8), b = 10.1053(9), c = 16.4454(14) Å, α = 100.476(7), β = 93.485(7), γ = 115.407(9) °, Z = 2 and V = 1313.0(2)Å3. The structure involves a network of inorganic parallel layers built up by P6O186− ring anions, NH3 groups and water molecules. Charge balance is achieved by the protonated amine which is trapped in the interlayer space and interacts with the organic framework through strong hydrogen bonding. The 13C, 15N and 31P CP-MAS NMR spectra are in agreement with the X-ray structure. The vibrational absorption bands were identified by infrared spectroscopy. DFT calculations allowed the attribution of the NMR peaks.

Complexes of Copper(I) Thiocyanate with Monodentate Phosphine and Pyridine Ligands and the P(,N)‐Donor Diphenyl(2‐pyridyl)phosphine

AbstractCopper(I) thiocyanate derivatives were prepared by the reaction of CuNCS with pyridine (py) and tertiary monophosphine ligands [PR3 in general; in detail: PPh3, triphenylphosphine, P(4‐FPh)3, tris(4‐fluorophenyl)phosphine)], as well as the potentially bidentate ligand diphenyl(2‐pyridyl)phosphine (PPh2py). Mechanochemical methods were used in some cases to investigate stoichieometries that were not easily accessible by conventional solution syntheses. Three forms of the resulting adducts of CuNCS/PR3/py‐base (1:3–n:n) stoichiometry―all containing four‐coordinate copper(I) atoms and monodentate N‐thiocyanate groups―were confirmed crystallographically. Mononuclear arrays are defined for [(PPh2py)3–n(py)nCuNCS], n = 0, 1, 2, the monodentate thiocyanate being N‐coordinated in all; two polymorphs are observed for the n = 2 complex, both crystallizing in monoclinic P21 (Z = 2) cells with similar cell dimensions, but with aromatic components eclipsed about the Cu–P bond in the PPh3 complex, and staggered in the PPh2py complex. Bridging thiocyanate groups are found in the 1:1:1 CuNCS/PPh2py/2‐methylpyridine (mpy) and P(4‐FPh)3/mpy complexes, wherein centrosymmetric dimers with eight‐membered central rings are obtained: [(R3P)(mpy)Cu(NCS)2Cu(PR3)(mpy)], as is also the case in the parent 1:2 CuNCS/PPh2py adduct [(pyPh2P)2Cu(NCS)2Cu(PPh2py)2]. For the 1:1:1 CuNCS/P(4‐FPh)3/py and PPh3/Brmpy (Brmpy = 3‐bromo‐4‐methylpyridine) adducts, and, likely, CuNCS/PPh2py/py (1:1:1), single‐stranded polymers of the form [···Cu(NCS)(PR3)(py‐base)(Cu)···](∞|∞) with linearly bridging NCS ligands were obtained. Some derivatives, representative of all forms, display medium to strong green to blue luminescence when excited with radiation at 365 nm. The 31P CPMAS NMR spectroscopic data clearly differentiate the inequivalent phosphorus positions within each system, showing a wide range of 1J(31P,63/65Cu) values ranging from 965 Hz for [Cu(NCS)(PPh2py)3] to 1540 Hz for dimeric [(4‐FPh)3P(mpy)Cu(NCS)2Cu(P(4‐FPh)3)(mpy)], reflecting the large variations in the Cu–P bond length.

Solid-state NMR structure characterization of a 13CO-Labeled Ir(I) complex with a P,N-donor ligand including ultrafast MAS methods.

The structural characterization of a (13)CO-labeled Ir(I) complex bearing an P,N-donor ligand (1-[2-(diphenylphosphino)ethyl]pyrazole), [Ir(PyP)((13)CO)Cl] is demonstrated using a series of tailored solid-state NMR techniques based on ultrafast (60 kHz) Magic Angle Spinning (MAS), which facilitates correlations with narrow proton line-widths. Our 1D (1)H MAS and 2D (13)C and (31)P CP-MAS NMR spectra provided structural information similar to that obtained using NMR spectroscopy in solution. We employed high-resolution 2D solid-state correlation spectroscopy ((1)H-(13)C HETCOR, (1)H-(31)P correlation) to characterize the networks of dipolar couplings between protons and carbon/phosphorus. (1)H-(1)H SQ-SQ correlation spectra showed the dipolar contacts between all protons in a similar fashion to its solution counterpart, NOESY. The use of the (1)H single quantum/double quantum experiments made it possible to observe the dipolar-coupling contacts between immediately adjacent protons. Additionally, internuclear (13)CO-(31)P distance measurements were performed using REDOR. The combination of all of these techniques made it possible to obtain comprehensive structural information on the molecule [Ir(PyP)((13)CO)Cl] in the solid state, which is in excellent agreement with the single crystal X-ray structure of the complex, and demonstrates the enormous value of ultrafast MAS NMR techniques for a broad range of future applications.

ChemInform Abstract: Monomer and Dimer of Mono‐titanium(IV)‐Containing α‐Keggin Polyoxometalates: Synthesis, Molecular Structures, and pH‐Dependent Monomer—Dimer Interconversion in Solution.

AbstractCompounds (III) and (IV) are characterized by single crystal XRD, FTIR, CPMAS 31P NMR, and solution 31P and 183W NMR spectroscopy.