# Nickel Complexes

**URL:** https://chemdotes.discourse.group/c/transition-metal-complexes/nickel-complexes/20.md

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## [About the Nickel Complexes category](https://chemdotes.discourse.group/t/about-the-nickel-complexes-category/55)

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

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

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**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")

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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…

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

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**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")

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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…