# Transition Metal Complexes

**URL:** https://chemdotes.discourse.group/c/transition-metal-complexes/7.md

[Latest](https://chemdotes.discourse.group/latest.md) · [Categories](https://chemdotes.discourse.group/categories.md) · [Tags](https://chemdotes.discourse.group/tags.md)

---

## [About the Transition Metal Complexes category](https://chemdotes.discourse.group/t/about-the-transition-metal-complexes-category/12)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0

</div>

Synthetic procedures and relevant data pertaining transition metal reagents, including lanthanides and actinides, for stoichiometric or catalytic applications, among others. Why should people use this reagent? What re…

---

## [Na2\[Fe(CO)4\] (Collman's reagent) (14878-31-0)](https://chemdotes.discourse.group/t/na2-fe-co-4-collmans-reagent-14878-31-0/72)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [April 11, 2024, 3:03am UTC](https://chemdotes.discourse.group/t/na2-fe-co-4-collmans-reagent-14878-31-0/72 "2024-04-11T03:03:37Z")

</div>

Sodium tetracarbonylferrate, better known as Collman’s reagent, is an electron-rich iron complex that has found use in organic synthesis. Namely, in the conversion of alkyl halides/sulfonates to carbonyl-containing compo…

---

## [Fe(acetylacetonate)3 (14024-18-1)](https://chemdotes.discourse.group/t/fe-acetylacetonate-3-14024-18-1/70)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [April 3, 2024, 3:47pm UTC](https://chemdotes.discourse.group/t/fe-acetylacetonate-3-14024-18-1/70 "2024-04-03T15:47:08Z")

</div>

Among all iron catalysts employed in organic synthesis, tris(acetylacetonato)iron(III) or Fe(acac)3 is one the most popular. This is, in part, because it is air stable, easy to make, and soluble in organic solvents. It h…

---

## [RhCl(PPh3)3 (Wilkinson's catalyst) (14694-95-2)](https://chemdotes.discourse.group/t/rhcl-pph3-3-wilkinsons-catalyst-14694-95-2/69)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 30, 2024, 11:37pm UTC](https://chemdotes.discourse.group/t/rhcl-pph3-3-wilkinsons-catalyst-14694-95-2/69 "2024-03-30T23:37:43Z")

</div>

Wilkinson’s catalyst is a burgundy-colored solid featuring a central rhodium(I) in a 16-electron, square-planar coordination environment. First reported by Osborn and Wilkinson in 1966,\[1\] the complex became a centerpiec…

---

## [Pd2(dibenzylideneacetone)3 (51364-51-3)](https://chemdotes.discourse.group/t/pd2-dibenzylideneacetone-3-51364-51-3/67)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 29, 2024, 3:49am UTC](https://chemdotes.discourse.group/t/pd2-dibenzylideneacetone-3-51364-51-3/67 "2024-03-29T03:49:39Z")

</div>

Palladium-based complexes comprise some of the most important catalysts in synthetic chemistry. Its ability to reliably and cyclically effect two-electron bond-forming and bond-breaking processes has made palladium the g…

---

## [Cu(acetonitrile)4 tetrafluoroborate (15418-29-8)](https://chemdotes.discourse.group/t/cu-acetonitrile-4-tetrafluoroborate-15418-29-8/63)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 26, 2024, 5:08am UTC](https://chemdotes.discourse.group/t/cu-acetonitrile-4-tetrafluoroborate-15418-29-8/63 "2024-03-26T05:08:01Z")

</div>

Copper(I) halide complexes such as CuI are routinely used in catalytic and material applications, such as catalysts in the Ullmann coupling and as p-type semiconductors, respectively.\[1\] However, these compounds typicall…

---

## [ThCl4(dimethoxyethane)2 (639084-65-4)](https://chemdotes.discourse.group/t/thcl4-dimethoxyethane-2-639084-65-4/61)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 25, 2024, 4:42am UTC](https://chemdotes.discourse.group/t/thcl4-dimethoxyethane-2-639084-65-4/61 "2024-03-25T04:42:17Z")

</div>

Among the actinides, uranium and thorium are the most abundant in the earth’s crust due their long-lived isotopes (thorium-232 and uranium-238). These tend to be found in the form of oxides such as thoria (ThO2) and uran…

---

## [FeBr2(dimethoxyethane) (99611-53-7)](https://chemdotes.discourse.group/t/febr2-dimethoxyethane-99611-53-7/60)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 24, 2024, 12:12am UTC](https://chemdotes.discourse.group/t/febr2-dimethoxyethane-99611-53-7/60 "2024-03-24T00:12:03Z")

</div>

Dihalide complexes of iron(II) have found use as a starting platform to more eleborate Fe(II) complexes, and as a catalyst in cross-coupling reactions.\[1\] A source of soluble iron(II) dihalide, FeBr2(dme) can be easily s…

---

## [RhCl(1,5-cyclooctadiene) dimer (12092-47-6)](https://chemdotes.discourse.group/t/rhcl-1-5-cyclooctadiene-dimer-12092-47-6/41)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 12, 2024, 12:20am UTC](https://chemdotes.discourse.group/t/rhcl-1-5-cyclooctadiene-dimer-12092-47-6/41 "2024-03-12T00:20:08Z")

</div>

RhCl(1,5-cyclooctadiene) dimer is a tremendously useful Rh(I) source due to its solubility in organic solvents and easy removal of the cyclooctadiene ligand for further derivatization. It is largely used for catalytic hy…

---

## [PtCl2(1,5-cyclooctadiene) (12080-32-9)](https://chemdotes.discourse.group/t/ptcl2-1-5-cyclooctadiene-12080-32-9/40)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 8, 2024, 7:19pm UTC](https://chemdotes.discourse.group/t/ptcl2-1-5-cyclooctadiene-12080-32-9/40 "2024-03-08T19:19:41Z")

</div>

Dichloro(1,5-cyclooctadiene)platinum(II) can be conveniently synthesized via the procedure from Holst et al.\[1\] Procedure: In air, a 100mL round-bottom flask was charged with a magnetic stir bar, potassium tetrachloropl…

---

## [FeCl2(pyridine)4 (Yellow salt) (15138-92-8)](https://chemdotes.discourse.group/t/fecl2-pyridine-4-yellow-salt-15138-92-8/49)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 19, 2024, 7:31pm UTC](https://chemdotes.discourse.group/t/fecl2-pyridine-4-yellow-salt-15138-92-8/49 "2024-03-19T19:31:48Z")

</div>

Soluble iron(II) dihalide complexes with labile ligands are useful sources of iron for a large number of applications: Catalytic reactions such as hydrogenation and hydroformylation, mechanistic studies, studies of trans…

---

## [NiCl2(dimethoxyethane) (29046-78-4)](https://chemdotes.discourse.group/t/nicl2-dimethoxyethane-29046-78-4/37)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 5, 2024, 5:03pm UTC](https://chemdotes.discourse.group/t/nicl2-dimethoxyethane-29046-78-4/37 "2024-03-05T17:03:11Z")

</div>

The most common source of nickel dihalide reagents are the hexahydrates, which tend to be poorly soluble in organic solvents. Furthermore, the use of nickel complexes in synthetic applications often requires anhydrous co…

---

## [NiBr2(dimethoxyethane) (28923-39-9)](https://chemdotes.discourse.group/t/nibr2-dimethoxyethane-28923-39-9/48)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 19, 2024, 5:49am UTC](https://chemdotes.discourse.group/t/nibr2-dimethoxyethane-28923-39-9/48 "2024-03-19T05:49:20Z")

</div>

Although simple nickel dihalides may seem as attractive Ni(II) sources in organometallic/transition-metal chemistry, they exhibit poor solubility in organic solvents. Furthermore, the use of nickel complexes in synthetic…

---

## [CoBr2(dimethoxyethane) (18346-57-1)](https://chemdotes.discourse.group/t/cobr2-dimethoxyethane-18346-57-1/51)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 21, 2024, 4:35pm UTC](https://chemdotes.discourse.group/t/cobr2-dimethoxyethane-18346-57-1/51 "2024-03-21T16:35:36Z")

</div>

Dihalide complexes of cobalt(II) have found use as catalysts in a variety of organic transformations. For example, C-N and C-C cross coupling reactions (Buchwald-Hartwig, Susuki, Kumada, Heck), functional group transfor…

---

## [NbCl3(dimethoxyethane) (110615-13-9)](https://chemdotes.discourse.group/t/nbcl3-dimethoxyethane-110615-13-9/43)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 13, 2024, 3:34am UTC](https://chemdotes.discourse.group/t/nbcl3-dimethoxyethane-110615-13-9/43 "2024-03-13T03:34:49Z")

</div>

NbCl3(dme) provides a convenient gateway into niobium(III) complexes. Due to its d2 configuration, it tends to exhibit Lewis basic behavior towards pi-ligands such as olefins. These types of complexes have found use in …

---

## [NbCl4(tetrahydrofuran)2 (61247-57-2)](https://chemdotes.discourse.group/t/nbcl4-tetrahydrofuran-2-61247-57-2/44)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 13, 2024, 6:47pm UTC](https://chemdotes.discourse.group/t/nbcl4-tetrahydrofuran-2-61247-57-2/44 "2024-03-13T18:47:36Z")

</div>

NbCl4(thf)2 provides a convenient gateway into niobium(IV) complexes due to its easily displaced THF ligands. While the chemistry of these types of complexes is underexplored, Nb(IV) has found use in reductive homocoupli…

---

## [NbCl2(pyridine)4 (168701-43-7)](https://chemdotes.discourse.group/t/nbcl2-pyridine-4-168701-43-7/45)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 14, 2024, 4:53pm UTC](https://chemdotes.discourse.group/t/nbcl2-pyridine-4-168701-43-7/45 "2024-03-14T16:53:19Z")

</div>

NbCl2(pyridine)4 provides a practical gateway into niobium(II) chemistry, a very rare oxidation state for the element. It can be synthesized via reduction according to the procedure of Cotton and Murillo.\[1\] Procedure: …

---

## [Nb(mesitylene)2 (68088-96-0)](https://chemdotes.discourse.group/t/nb-mesitylene-2-68088-96-0/46)

<div class="topic-metadata">

**Author:** [@bmpuerta](https://chemdotes.discourse.group/u/bmpuerta)\
**Replies:** 0\
**Last updated:** [March 15, 2024, 7:50pm UTC](https://chemdotes.discourse.group/t/nb-mesitylene-2-68088-96-0/46 "2024-03-15T19:50:43Z")

</div>

Nb(mesitylene)2 is a rare instance of niobium(0). This deep red, paramagnetic, 17 valence-electron complex has been used in the materials community as a source of niobium atoms for the synthesis of Nb-chalcogenide solids…
