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  2. Transition metal carbene complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_carbene...

    The Ta−CH 3 and Ta=CH 2 distances are 2.37 and 2.04 Å, respectively. Color code: blue = Ta, gray = C, white = H. Schrock carbenes do not have π-accepting ligands on the metal centre. They are often called alkylidene complexes. Typically this subset of carbene complexes are found with: [6] high oxidation state metal center

  3. Transition metal isocyanide complexes - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_iso...

    This advantage is illustrated by the isolation of the homoleptic vanadium hexaisocyanide complex in three oxidation states, i.e., [V(CNC 6 H 3-2,6-Me 2) 6] n for n = -1, 0, +1. [ 11 ] Because isocyanides are more basic donors ligands than CO, their complexes are susceptible to oxidation and protonation.

  4. Iron(III) chloride - Wikipedia

    en.wikipedia.org/wiki/Iron(III)_chloride

    Fe 2 O 3 + 6 HCl + 9 H 2 O → 2 FeCl 3 (H 2 O) 6. In complementary route, iron metal can be oxidized by hydrochloric acid followed by chlorination: [10] Fe + 2 HCl → FeCl 2 + H 2 FeCl 2 + 0.5 Cl 2 + 6 H 2 O → FeCl 3 (H 2 O) 6. A number of variables apply to these processes, including the oxidation of iron by ferric chloride and the ...

  5. Transition metal porphyrin complexes - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_porphyrin...

    MCl x + H 2 P → M(P)Cl 2−x + 2 HCl. Two pyrrole protons are lost. The porphyrin dianion is an L 2 X 2 ligand. These syntheses require somewhat forcing conditions, [9] consistent with the tight fit of the metal in the N 4 2-"pocket." In nature, the insertion is mediated by chelatase enzymes. The insertion of a metal proceeds by the ...

  6. Ligand - Wikipedia

    en.wikipedia.org/wiki/Ligand

    A classic bidentate ligand is ethylenediamine, which is derived by the linking of two ammonia groups with an ethylene (−CH 2 CH 2 −) linker. A classic example of a polydentate ligand is the hexadentate chelating agent EDTA , which is able to bond through six sites, completely surrounding some metals.

  7. Boranes - Wikipedia

    en.wikipedia.org/wiki/Boranes

    B 2 H 6 + 2 CH 2 =CHR → 2 BH 2 (CH 2 CH 2 R) B 2 H 6 + 4 CH 2 =CHR → 2 BH(CH 2 CH 2 R) 2 B 2 H 6 + 6 CH 2 =CHR → 2 B(CH 2 CH 2 R) 2. Alkyl and aryl boranes can also be produced by alkylation of chloroboranes and boronic esters.

  8. VSEPR theory - Wikipedia

    en.wikipedia.org/wiki/VSEPR_theory

    Another example is O(SiH 3) 2 with an Si–O–Si angle of 144.1°, which compares to the angles in Cl 2 O (110.9°), (CH 3) 2 O (111.7°), and N(CH 3) 3 (110.9°). [24] Gillespie and Robinson rationalize the Si–O–Si bond angle based on the observed ability of a ligand's lone pair to most greatly repel other electron pairs when the ligand ...

  9. Metal cluster compound - Wikipedia

    en.wikipedia.org/wiki/Metal_cluster_compound

    One example is Zr 6 CCl 12. [7] One structure type features six terminal halides and 12 edge-bridging halides. This motif is exemplified by tungsten(III) chloride, [Ta 6 Cl 18] 4−, [8] Another common structure has six terminal halides and 8 bridging halides, e.g. Mo 6 Cl 14 2−. Structure of edge-capped octahedral clusters such as Ta 6 Cl 18 ...