To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

2-(Dicyanomethylene)croconate

From Wikipedia, the free encyclopedia

2-(Dicyanomethylene)croconate
2-(dicyanomethylene)croconate dianion
Names
Preferred IUPAC name
4-(Dicyanomethylene)-3,5-dioxo-1-cyclopentene-1,2-diolate
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C8H2N2O4/c9-1-3(2-10)4-5(11)7(13)8(14)6(4)12/h13-14H/p-2 checkY
    Key: UOFODKSWJURJDQ-UHFFFAOYSA-L checkY
  • C(#N)C(=C1C(=O)C(=C(C1=O)[O-])[O-])C#N
Properties
C8N2O42−
Molar mass 188.099 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

2-(Dicyanomethylene)croconate is a divalent anion with chemical formula C
8
N
2
O2−
4
or ((N≡C−)2C=)(C5O4)2−. It is one of the pseudo-oxocarbon anions, as it can be described as a derivative of the croconate oxocarbon anion C
5
O2−
5
through the replacement of one oxygen atom by a dicyanomethylene group =C(−C≡N)2.

The anion was synthesized and characterized by A. Fatiadi in 1980, by hydrolysis of croconate violet treated with potassium hydroxide.[1] It gives an orange solution in water.

See also

References

  1. ^ Alexander J. Fatiadi (1980), "Pseudooxocarbons. Synthesis of 1,2,3-tris(dicyanomethylene)croconate salts. A new bond-delocalized dianion, croconate blue". Journal of Organic Chemistry volume 45, pages 1338–1339. doi:10.1021/jo01295a044
This page was last edited on 23 April 2023, at 11:51
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.