The activation of small molecules using frustrated Lewis pairs

This thesis describes the activation of small molecules using frustrated Lewis pairs, in particular investigating their use to reduce CO₂ to methanol, thus producing a new route towards a renewable fuel.Chapter One summarises the requirement for a renewable fuel source, the alternative methods currently available and previous research conducted into converting CO₂ to methanol using FLPs and other reducing agents.Chapter Two describes the synthesis of a new family of electron-deficient tris(aryl)boranes, B(C₆F₅)3-x(C₆Cl₅)x (x = 1-3), allowing the electronic effects, resulting from the gradual replacement of C₆F₅ with C₆Cl₅ ligands, to be studied. The novel Lewis acids have been fully characterised and their Lewis acidities have been determined using NMR spectroscopy, electrochemistry and DFT studies.Chapter Three discusses the synthesis of nine novel FLPs and their use to successfully split H2. Each borohydride salt has been spectroscopically fully characterised and five of the salts have been characterised using single crystal X-ray diffraction. To determine the exact positions of the H atoms, single crystal neutron diffraction and DFT experiments were carried out on [1-H][H-TMP].Chapter Four details attempts to use the borohydride salts, synthesised in Chapter Three, to reduce CO₂ to methanol. Each experiment was been fully investigated and their catalytic viability was determined. The X-ray crystal structure of [1-OCHO][H-TMP] is described and each formatoborate and methoxyborate salt were fully characterised.Chapter Five describes experimental procedures and characterisation data.</p

The activation of small molecules using frustrated Lewis pairs

This thesis describes the activation of small molecules using frustrated Lewis pairs, in particular investigating their use to reduce CO₂ to methanol, thus producing a new route towards a renewable fuel. Chapter One summarises the requirement for a renewable fuel source, the alternative methods currently available and previous research conducted into converting CO₂ to methanol using FLPs and other reducing agents. Chapter Two describes the synthesis of a new family of electron-deficient tris(aryl)boranes, B(C₆F₅)3-x(C₆Cl₅)x (x = 1-3), allowing the electronic effects, resulting from the gradual replacement of C₆F₅ with C₆Cl₅ ligands, to be studied. The novel Lewis acids have been fully characterised and their Lewis acidities have been determined using NMR spectroscopy, electrochemistry and DFT studies. Chapter Three discusses the synthesis of nine novel FLPs and their use to successfully split H2. Each borohydride salt has been spectroscopically fully characterised and five of the salts have been characterised using single crystal X-ray diffraction. To determine the exact positions of the H atoms, single crystal neutron diffraction and DFT experiments were carried out on [1-H][H-TMP]. Chapter Four details attempts to use the borohydride salts, synthesised in Chapter Three, to reduce CO₂ to methanol. Each experiment was been fully investigated and their catalytic viability was determined. The X-ray crystal structure of [1-OCHO][H-TMP] is described and each formatoborate and methoxyborate salt were fully characterised. Chapter Five describes experimental procedures and characterisation data.EThOS - Electronic Theses Online ServiceGBUnited Kingdo

Structural and theoretical studies of intermolecular dihydrogen bonding in [(C6F5)2(C6Cl5)B]–H...H–[TMP]

The product of the intermolecular ‘frustrated Lewis pair’ (FLP) B(C6F5)2(C6Cl5)/2,2,6,6-tetramethylpiperidine and H2 has been studied by single-crystal neutron diffraction. This is the first structurally characterised example of a geometrically unconstrained dihydrogen (H⋯H) bond within a hydrogenated FLP system

Separating Electrophilicity and Lewis Acidity: The Synthesis, Characterization, and Electrochemistry of the Electron Deficient Tris(aryl)boranes B(C6F5)3–n(C6Cl5)n (n= 1–3)

A new family of electron-deficient tris(aryl)boranes, B(C(6)F(5))(3-n)(C(6)Cl(5))(n) (n = 1-3), has been synthesized, permitting an investigation into the steric and electronic effects resulting from the gradual replacement of C(6)F(5) with C(6)Cl(5) ligands. B(C(6)F(5))(2)(C(6)Cl(5)) (3) is accessed via C(6)Cl(5)BBr(2), itself prepared from donor-free Zn(C(6)Cl(5))(2) and BBr(3). Reaction of C(6)Cl(5)Li with BCl(3) in a Et(2)O/hexane slurry selectively produced B(C(6)Cl(5))(2)Cl, which undergoes B-Cl exchange with CuC(6)F(5) to afford B(C(6)F(5))(C(6)Cl(5))(2) (5). While 3 forms a complex with H(2)O, which can be rapidly removed under vacuum or in the presence of molecular sieves, B(C(6)Cl(5))(3) (6) is completely stable to refluxing toluene/H(2)O for several days. Compounds 3, 5, and 6 have been structurally characterized using single crystal X-ray diffraction and represent the first structure determinations for compounds featuring B-C(6)Cl(5) bonds; each exhibits a trigonal planar geometry about B, despite having different ligand sets. The spectroscopic characterization using (11)B, (19)F, and (13)C NMR indicates that the boron center becomes more electron-deficient as n increases. Optimized structures of B(C(6)F(5))(3-n)(C(6)Cl(5))(n) (n = 0-3) using density functional theory (B3LYP/TZVP) are all fully consistent with the experimental structural data. Computed (11)B shielding constants also replicate the experimental trend almost quantitatively, and the computed natural charges on the boron center increase in the order n = 0 (0.81) < n = 1 (0.89) < n = 2 (1.02) < n = 3 (1.16), supporting the hypothesis that electrophilicity increases concomitantly with substitution of C(6)F(5) for C(6)Cl(5). The direct solution cyclic voltammetry of B(C(6)F(5))(3) has been obtained for the first time and electrochemical measurements upon the entire series B(C(6)F(5))(3-n)(C(6)Cl(5))(n) (n = 0-3) corroborate the spectroscopic data, revealing C(6)Cl(5) to be a more electron-withdrawing group than C(6)F(5), with a ca. +200 mV shift observed in the reduction potential per C(6)F(5) group replaced. Conversely, use of the Guttmann-Beckett and Childs' methods to determine Lewis acidity on B(C(6)F(5))(3), 3, and 5 showed this property to diminish with increasing C(6)Cl(5) content, which is attributed to the steric effects of the bulky C(6)Cl(5) substituents. This conflict is ascribed to the minimal structural reorganization in the radical anions upon reduction during cyclic voltammetric experiments. Reduction of 6 using Na((s)) in THF results in a vivid blue paramagnetic solution of Na(+) [6](•-); the EPR signal of Na(+)[6](•-) is centered at g = 2.002 with a((11)B) 10G. Measurements of the exponential decay of the EPR signal (298 K) reveal [6](•-) to be considerably more stable than its perfluoro analogue