
Regolith Geochemistry & Mineralogy
... unsatisfied bonds at crystal surface and edges • Some clay minerals also have permanent negative charges due to T and O substitutions • These charges attract cations or anions that bond (adsorb or ion exchange) to the surface ions is specific ways – surface complexes ...
... unsatisfied bonds at crystal surface and edges • Some clay minerals also have permanent negative charges due to T and O substitutions • These charges attract cations or anions that bond (adsorb or ion exchange) to the surface ions is specific ways – surface complexes ...
Low-valent titanium: New synthetic applications
... 3. Vnusual orrho-hydrosgl-assisted reduction of aromatic alkenes In our attempts to exrend the above protocol ro the synthesis of 2.3-dialkylbenzo[b]luram. i: n a s logical to use 2'-acetoxyacetophenone (5) as substrate. To our surprise, 2.3-dimerhylbenzo[b]furan ( 6 ) was not formed hut diarylalkan ...
... 3. Vnusual orrho-hydrosgl-assisted reduction of aromatic alkenes In our attempts to exrend the above protocol ro the synthesis of 2.3-dialkylbenzo[b]luram. i: n a s logical to use 2'-acetoxyacetophenone (5) as substrate. To our surprise, 2.3-dimerhylbenzo[b]furan ( 6 ) was not formed hut diarylalkan ...
Tuning the Bergman Cyclization by Introduction of Metal Fragments
... slightly nonplanar, making 8 chiral. The barrier to its racemization is computed as only 4 kcal/mol.31 Should we make something of the localization of C-C bonds in this osmabenzyne 8? It should be good to know the extent of localization in metallabenzenes.8,13 This is not easy to come by, as many of ...
... slightly nonplanar, making 8 chiral. The barrier to its racemization is computed as only 4 kcal/mol.31 Should we make something of the localization of C-C bonds in this osmabenzyne 8? It should be good to know the extent of localization in metallabenzenes.8,13 This is not easy to come by, as many of ...
One-Electron Transformations of Paramagnetic Cobalt
... alkyls range from 1.9 to 2.2 µB, consistent with a low-spin d7 center (one unpaired electron) with some second-order spinorbit coupling.35 This confirms that a geometry change from tetrahedral to square planar has occurred. It should be noted that the geometry of the cyclopentadienyl complex 7 is in ...
... alkyls range from 1.9 to 2.2 µB, consistent with a low-spin d7 center (one unpaired electron) with some second-order spinorbit coupling.35 This confirms that a geometry change from tetrahedral to square planar has occurred. It should be noted that the geometry of the cyclopentadienyl complex 7 is in ...
WM Att/a
... a metal ?uoride to an ether-boron tri?uoride complex, fol complex is less than the bond strength of the desired ?uo lowed by liberation of ether. Fluoborates in comparison with corresponding anhydrous metal ?uoride-B113 com 55 borate. To a degree this principle was recognized by the teachings of the ...
... a metal ?uoride to an ether-boron tri?uoride complex, fol complex is less than the bond strength of the desired ?uo lowed by liberation of ether. Fluoborates in comparison with corresponding anhydrous metal ?uoride-B113 com 55 borate. To a degree this principle was recognized by the teachings of the ...
Monocopper Doping in Cd-In-S Supertetrahedral Nanocluster via
... quaternary Cu2ZnSnS4 colloidal nanocrystals similar in size to the T5 cluster.14 An octahedral crystal of ISC-10-CdInS was synthesized by solvothermal reaction of Cd(NO3)2, indium, and sulfur in the mixed solvents of 1,5-diazabicyclo[4.3.0]non-5-ene (DBN), piperidine (PR), and water at 190 °C for 12 ...
... quaternary Cu2ZnSnS4 colloidal nanocrystals similar in size to the T5 cluster.14 An octahedral crystal of ISC-10-CdInS was synthesized by solvothermal reaction of Cd(NO3)2, indium, and sulfur in the mixed solvents of 1,5-diazabicyclo[4.3.0]non-5-ene (DBN), piperidine (PR), and water at 190 °C for 12 ...
Chemistry 5325/5326 Inorganic Chemistry Spring Semester 2012
... First-row transition metals may be either low spin or high spin. Because tetrahedral complexes have much smaller d-orbital splitting (∆t ) than octahedral complexes (∆0 ), almost all tetrahedral first-row transition metal complexes are high spin. For octahedral complexes, the nature of the ligand pl ...
... First-row transition metals may be either low spin or high spin. Because tetrahedral complexes have much smaller d-orbital splitting (∆t ) than octahedral complexes (∆0 ), almost all tetrahedral first-row transition metal complexes are high spin. For octahedral complexes, the nature of the ligand pl ...
non-metal chemistry notes
... compounds with unpaired electrons (e.g. NO, NO2, ClO2). Radicals are not frequently found amongst the p-block however, as the s-p hybrid orbitals that usually form in these compounds have fairly good directional overlap, so reasonably strong bonds are formed such that any radical species tend to dim ...
... compounds with unpaired electrons (e.g. NO, NO2, ClO2). Radicals are not frequently found amongst the p-block however, as the s-p hybrid orbitals that usually form in these compounds have fairly good directional overlap, so reasonably strong bonds are formed such that any radical species tend to dim ...
communications - University of Notre Dame
... the aid of cryptated alkali metal countercations.[2] The recently reported phases A4E9 and A12E17 (A K, Rb, or Cs; E Si, Ge, Sn, or Pb) contain isolated E94ÿ deltahedra and extend the range of existence of large clusters of this group to the solid state.[3] According to Wades rules for counting ...
... the aid of cryptated alkali metal countercations.[2] The recently reported phases A4E9 and A12E17 (A K, Rb, or Cs; E Si, Ge, Sn, or Pb) contain isolated E94ÿ deltahedra and extend the range of existence of large clusters of this group to the solid state.[3] According to Wades rules for counting ...
A sensitive method to screen for hydroxyl radical scavenging activity
... natural food extracts are shown in Table 2. Based on percent inhibition of 8-OH dG formed, each test substance was graded in an arbitrary five point scale. Representative antioxidants screened in this study, such as bovine serum albumin, cysteine and glutathione (GSH) scored a 4-t grade in hydroxyl ...
... natural food extracts are shown in Table 2. Based on percent inhibition of 8-OH dG formed, each test substance was graded in an arbitrary five point scale. Representative antioxidants screened in this study, such as bovine serum albumin, cysteine and glutathione (GSH) scored a 4-t grade in hydroxyl ...
Reaction Mechanism of d-metal complexes Chapter 20
... n most substitution pathways: bond formation with Y and bond breaking with X is concurrent. In the I (interchange) mechanism: no intermediate phase but various transition states: dissociative interchange (Id) bond breaking dominates bond forming associative interchange (Ia) bond formation dominates ...
... n most substitution pathways: bond formation with Y and bond breaking with X is concurrent. In the I (interchange) mechanism: no intermediate phase but various transition states: dissociative interchange (Id) bond breaking dominates bond forming associative interchange (Ia) bond formation dominates ...
Fulltext: english, pdf
... Figure 3. FTIR spectra of (A) Compound 1; (B) Compound 2; (C) Compound 3; (D) Compound 4; (E) Compound 5; and their complexes with Ca2+ ion. mainly β- and γ- turn.[38] In the presence of Cu2+ the ECD spectrum shows a strong, very broad negative band centered at ~ 200 nm and a weaker one at ~ 240 nm. ...
... Figure 3. FTIR spectra of (A) Compound 1; (B) Compound 2; (C) Compound 3; (D) Compound 4; (E) Compound 5; and their complexes with Ca2+ ion. mainly β- and γ- turn.[38] In the presence of Cu2+ the ECD spectrum shows a strong, very broad negative band centered at ~ 200 nm and a weaker one at ~ 240 nm. ...
High Mass Resolution Plasma Desorption and
... The N i-N i distances of 2.919Ä, excluding strong m etal-m etal interactions, and the N i-S bond lengths with a mean of 2.201 Ä are com parable to the corresponding values in other known cyclic hexanuclear nickel thiolate complexes [18- 23]. S I emission Since both dried sample solutions and crystal ...
... The N i-N i distances of 2.919Ä, excluding strong m etal-m etal interactions, and the N i-S bond lengths with a mean of 2.201 Ä are com parable to the corresponding values in other known cyclic hexanuclear nickel thiolate complexes [18- 23]. S I emission Since both dried sample solutions and crystal ...
Electronic structure of a neutral oxygen vacancy in SrTiO3
... set is (8s5p5d/3s3 p3d). 29 For the Sr atoms we used an ECP which includes in the valence the 4s 2 4p 6 5s 2 electrons and a (8s6 p/3s3 p) basis set.29 A problem in the study of vacancies with atomic basis functions is that these are associated with the atomic nuclei. When an atom is removed, the sp ...
... set is (8s5p5d/3s3 p3d). 29 For the Sr atoms we used an ECP which includes in the valence the 4s 2 4p 6 5s 2 electrons and a (8s6 p/3s3 p) basis set.29 A problem in the study of vacancies with atomic basis functions is that these are associated with the atomic nuclei. When an atom is removed, the sp ...
Mass spectra and structures of Cu Rg nclusters (Rg ¼ Ne, Ar)
... for Auþ Rg have also been carried out [22,23] and show the formation of covalent character bonds for the heavier inert gas atoms. Cuþ has a fully occupied d orbital ðd10 Þ electronic configuration and it is interesting to investigate its complexes with noble gas atoms and compare them with those of a ...
... for Auþ Rg have also been carried out [22,23] and show the formation of covalent character bonds for the heavier inert gas atoms. Cuþ has a fully occupied d orbital ðd10 Þ electronic configuration and it is interesting to investigate its complexes with noble gas atoms and compare them with those of a ...
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).