
NOMENCLATURE OF ORGANOMETALLIC COMPOUNDS OF THE
... inevitable electron book-keeping that ensues upon consideration of a chemical compound, the coordination entity was dissected (in thought) by removing each ligand in such a way that each ligating atom or group took two electrons with it. This de®nition is now no longer appropriate in all those areas ...
... inevitable electron book-keeping that ensues upon consideration of a chemical compound, the coordination entity was dissected (in thought) by removing each ligand in such a way that each ligating atom or group took two electrons with it. This de®nition is now no longer appropriate in all those areas ...
Low Thermal Mass Gas Chromatography: Principles and Applications
... Principle and design of LTMGC smaller heater plates, internal heater wire, and a resistively Temperature programming is often conducted by electronic heated element with a column in a sheath. temperature control of an oven that houses the GC column. In theory, resistively heated temperature programm ...
... Principle and design of LTMGC smaller heater plates, internal heater wire, and a resistively Temperature programming is often conducted by electronic heated element with a column in a sheath. temperature control of an oven that houses the GC column. In theory, resistively heated temperature programm ...
Title
... are longer than those found in their crystal structures, being the largest deviations for the Ru-P bonds (1: 9%; 2: 8%) and Ru-N (1, 2: 4%) (Table S2 and S8 in Supporting Information). The optimized bpy rings are less distorted than in the crystal structures and the ligands PTA are rotated around th ...
... are longer than those found in their crystal structures, being the largest deviations for the Ru-P bonds (1: 9%; 2: 8%) and Ru-N (1, 2: 4%) (Table S2 and S8 in Supporting Information). The optimized bpy rings are less distorted than in the crystal structures and the ligands PTA are rotated around th ...
Studies on Veratryl Alcohol Oxidation Catalyzed by Co(salen) Type
... rational catalyst design it is imperative to understand the catalytic process in detail. In this thesis Co(salen) [salen = N,N’-bis(salicylidene)ethylenediamine] type complexes were studied as oxygen activators for the selective oxidation of a lignin model compound using water as the solvent and mol ...
... rational catalyst design it is imperative to understand the catalytic process in detail. In this thesis Co(salen) [salen = N,N’-bis(salicylidene)ethylenediamine] type complexes were studied as oxygen activators for the selective oxidation of a lignin model compound using water as the solvent and mol ...
Investigating the Dearomative Rearrangement of Biaryl Phosphine- Ligated Pd(II) Complexes
... ring of biaryl phosphine ligands may not be innocent in the reactivity and decomposition pathways of catalytic intermediates. Reactions wherein a transition metal-bound arene undergoes nucleophilic attack are well-established,18 as are a number of dearomatization reactions using Pd and Pt catalysts. ...
... ring of biaryl phosphine ligands may not be innocent in the reactivity and decomposition pathways of catalytic intermediates. Reactions wherein a transition metal-bound arene undergoes nucleophilic attack are well-established,18 as are a number of dearomatization reactions using Pd and Pt catalysts. ...
Manfred Scheer Coordination Chemistry of Phosphorous
... structure, minor product with closo structure ...
... structure, minor product with closo structure ...
Structural Characterization of Natural Nickel and Copper
... Organic ligands form strong complexes with many trace elements in seawater. Various metals can compete for the same ligand chelation sites, and the final speciation of bound metals is determined by relative binding affinities, concentrations of binding sites, uncomplexed metal concentrations, and as ...
... Organic ligands form strong complexes with many trace elements in seawater. Various metals can compete for the same ligand chelation sites, and the final speciation of bound metals is determined by relative binding affinities, concentrations of binding sites, uncomplexed metal concentrations, and as ...
From concentrated metal solutions to crystalline electrides
... The first electride, Cs+(18C6)2-e-, (refs. 38-41) contains electrons that are trapped in a relatively deep (4.9 eV) potential well, interact only weakly with each other, and have very low spin density at the cesium nucleus. These features are deduced from a number of different measurements. The opti ...
... The first electride, Cs+(18C6)2-e-, (refs. 38-41) contains electrons that are trapped in a relatively deep (4.9 eV) potential well, interact only weakly with each other, and have very low spin density at the cesium nucleus. These features are deduced from a number of different measurements. The opti ...
PARAMAGNETIC RELAXATION REAGENTS HANS G
... a liquid there will be a modulation of the local magnetic field and this provides a mechanism for relaxation. Such a mechanism is pronounced for nuclei with large chemical shift ranges like ^c, 15 15N,16 19pl7 and 31p# Machor showed an unambiguous example of CSA relaxation for 19F in CHFC12.18 This ...
... a liquid there will be a modulation of the local magnetic field and this provides a mechanism for relaxation. Such a mechanism is pronounced for nuclei with large chemical shift ranges like ^c, 15 15N,16 19pl7 and 31p# Machor showed an unambiguous example of CSA relaxation for 19F in CHFC12.18 This ...
Characteristics of Gold Biosorption from Cyanide Solution
... in solution may be required to neutralize the extra-negative charge of the bonded selenate (SeO42-). This is responsible for the optimum pH for selenate uptake being a little lower than that observed for the uptake of monovalent anion AuCN-. When pH<3, chloride ions start strongly competing for acti ...
... in solution may be required to neutralize the extra-negative charge of the bonded selenate (SeO42-). This is responsible for the optimum pH for selenate uptake being a little lower than that observed for the uptake of monovalent anion AuCN-. When pH<3, chloride ions start strongly competing for acti ...
Chapter 4 - DiVA portal
... In the photosynthetic process in green plants, algae and cyanobacteria, sunlight is absorbed and converted into chemical energy [1]. The reactions responsible for this process is a series of highly efficient energy and electron transfer steps that results in the formation of energy rich compounds fr ...
... In the photosynthetic process in green plants, algae and cyanobacteria, sunlight is absorbed and converted into chemical energy [1]. The reactions responsible for this process is a series of highly efficient energy and electron transfer steps that results in the formation of energy rich compounds fr ...
Experiment 6 Porphyrins
... system of alternating single and double bonds (conjugated ʌ-system) of the chlorophyll porphyrin ring. The complexed magnesium metal ion acts to: x help make the entire structure rigid, thus minimising the energy lost as heat via molecular vibrations; x enhance the rate at which energy is transferre ...
... system of alternating single and double bonds (conjugated ʌ-system) of the chlorophyll porphyrin ring. The complexed magnesium metal ion acts to: x help make the entire structure rigid, thus minimising the energy lost as heat via molecular vibrations; x enhance the rate at which energy is transferre ...
The Organogallium Subhalide R Ga I as Starting Compound for the
... (δ < 30) [12]. Similar shifts were observed for the related transition metal GaR complexes cited above [6]. An even stronger shift to lower field (δ > 62) was detected for the tetrahedral clusters E 4 [C(SiMe3 )3 ]4 (E = Ga, In) [13, 14], which was explained by the particular bonding situation with ...
... (δ < 30) [12]. Similar shifts were observed for the related transition metal GaR complexes cited above [6]. An even stronger shift to lower field (δ > 62) was detected for the tetrahedral clusters E 4 [C(SiMe3 )3 ]4 (E = Ga, In) [13, 14], which was explained by the particular bonding situation with ...
Photoredox Catalysis Unlocks Single
... single-electron reductants.4−6 By employing catalysts with absorption bands in the visible region of the spectrum (rather than in the ultraviolet), the source of open shell intermediates can be effectively controlled.7,8 The rapid pace of recent developments combining photocatalysis with transition m ...
... single-electron reductants.4−6 By employing catalysts with absorption bands in the visible region of the spectrum (rather than in the ultraviolet), the source of open shell intermediates can be effectively controlled.7,8 The rapid pace of recent developments combining photocatalysis with transition m ...
01.Coligative properties of biological liquids.Complex compounds
... • H2O, CN-, NH3, NO2-, SCN-, OH-, X(halides), CO, O2– Example Complexes • [Co(NH3)6]Cl3 • K3 [Fe(SCN)6] ...
... • H2O, CN-, NH3, NO2-, SCN-, OH-, X(halides), CO, O2– Example Complexes • [Co(NH3)6]Cl3 • K3 [Fe(SCN)6] ...
Size match between cation and host cavity Electrostatic charge
... More flexible hosts can change easily from solvation to host complexation (without the need to pass through unstable intermediates) Macrocyclic molecules naturally tend to adopt their conformations so that no empty space remains inside the molecule When the structure is macrocyclic and very rigid so ...
... More flexible hosts can change easily from solvation to host complexation (without the need to pass through unstable intermediates) Macrocyclic molecules naturally tend to adopt their conformations so that no empty space remains inside the molecule When the structure is macrocyclic and very rigid so ...
Iron Complexes of C- and N-Methylated 2-Aza-21
... Insertion of iron(II) into methylated derivatives of N-confused porphyrins 2-aza-2-methyl-5,10,15,20-tetraphenyl-21carbaporphyrin (MeCTPPH)H, 2-aza-5,10,15,20-tetraphenyl-21-methyl-21-carbaporphyrin (CTPPMe)H2, and 2-aza2-methyl-5,10,15,20-tetraphenyl-21-methyl-21-carbaporphyrin (MeCTPPMe)H yielded ...
... Insertion of iron(II) into methylated derivatives of N-confused porphyrins 2-aza-2-methyl-5,10,15,20-tetraphenyl-21carbaporphyrin (MeCTPPH)H, 2-aza-5,10,15,20-tetraphenyl-21-methyl-21-carbaporphyrin (CTPPMe)H2, and 2-aza2-methyl-5,10,15,20-tetraphenyl-21-methyl-21-carbaporphyrin (MeCTPPMe)H yielded ...
Spin crossover

Spin Crossover (SCO), sometimes referred to as spin transition or spin equilibrium behavior, is a phenomenon that occurs in some metal complexes wherein the spin state of the complex changes due to external stimuli such as a variation of temperature, pressure, light irradiation or an influence of a magnetic field.With regard to a ligand field and ligand field theory, the change in spin state is a transition from a low spin (LS) ground state electron configuration to a high spin (HS) ground state electron configuration of the metal’s d atomic orbitals (AOs), or vice versa. The magnitude of the ligand field splitting along with the pairing energy of the complex determines whether it will have a LS or HS electron configuration. A LS state occurs because the ligand field splitting (Δ) is greater than the pairing energy of the complex (which is an unfavorable process).Figure 1 is a simplified illustration of the metal’s d orbital splitting in the presence of an octahedral ligand field. A large splitting between the t2g and eg AOs requires a substantial amount of energy for the electrons to overcome the energy gap (Δ) to comply with Hund’s Rule. Therefore, electrons will fill the lower energy t2g orbitals completely before populating the higher energy eg orbitals. Conversely, a HS state occurs with weaker ligand fields and smaller orbital splitting. In this case the energy required to populate the higher levels is substantially less than the pairing energy and the electrons fill the orbitals according to Hund’s Rule by populating the higher energy orbitals before pairing with electrons in the lower lying orbitals. An example of a metal ion that can exist in either a LS or HS state is Fe3+ in an octahedral ligand field. Depending on the ligands that are coordinated to this complex the Fe3+ can attain a LS or a HS state, as in Figure 1.Spin crossover refers to the transitions between high to low, or low to high, spin states. This phenomenon is commonly observed with some first row transition metal complexes with a d4 through d7 electron configuration in an octahedral ligand geometry. Spin transition curves are a common representation of SCO phenomenon with the most commonly observed types depicted in Figure 2 in which γHS (the high-spin molar fraction) is plotted vs. T. The figure shows a gradual spin transition (left), an abrupt transition with hysteresis (middle) and a two-step transition (right). For a transition to be considered gradual, it typically takes place over a large temperature range, even up to several hundred K, whereas for a transition to be considered abrupt, it should take place within 10 K or less.These curves indicate that a spin transition has occurred in a metal complex as temperature changed. The gradual transition curve is an indication that not all metal centers within the complex are undergoing the transition at the same temperature. The abrupt spin change with hysteresis indicates a strong cooperativity, or “communication”, between neighboring metal complexes. In the latter case, the material is bistable and can exist in the two different spin states with a different range of external stimuli (temperature in this case) for the two phenomena, namely LS → HS and HS → LS. The two-step transition is relatively rare but is observed, for example, with dinuclear SCO complexes for which the spin transition in one metal center renders the transition in the second metal center less favorable.There are several types of spin crossover that can occur in a complex; some of them are light induced excited state spin trapping (LIESST), ligand-driven light induced spin change (LD-LISC), and charge transfer induced spin transition (CTIST).