Lithium monoxide anion

{{Chembox

| Verifiedfields = changed

| Watchedfields = changed

| verifiedrevid = 459445215

| ImageFile =

| ImageFile2 =

| ImageSize = 240

| IUPACName = Lithium monoxide anion

| OtherNames = Lithate

|Section1={{Chembox Identifiers

| CASNo = 64538-53-0

| CASNo_Ref ={{cite web |title=Lithium oxide anion |url=https://webbook.nist.gov/cgi/formula?ID=C64538530 |website=webbook.nist.gov |language=en}}

| SMILES = [Li]-[O-]

| StdInChI=1S/Li.O/q;-1

| StdInChIKey = IXZJKKSRIFXCQD-UHFFFAOYSA-N

}}

|Section2={{Chembox Properties

| Li=1|O=1|Formula_Charge=-

| ConjugateAcid = Lithium hydroxide

}}

|Section3={{Chembox Hazards

| MainHazards = Extremely corrosive

}}

|Section4={{Chembox Related

| OtherFunction_label = bases

| OtherFunction = {{unbulleted list|

}}

}}

}}

Lithium monoxide anion ({{chem2|LiO−}}) is a superbase existing in the gas phase. It was the strongest known base until 2008, when the isomeric diethynylbenzene dianions were determined to have a higher proton affinity. The methanide ion {{chem2|CH3−}} was the strongest known base before lithium monoxide anion was discovered.{{cite journal |last1=Poad |first1=Berwyck L. J. |last2=Reed |first2=Nicholas D. |last3=Hansen |first3=Christopher S. |last4=Trevitt |first4=Adam J. |last5=Blanksby |first5=Stephen J. |last6=Mackay |first6=Emily G. |last7=Sherburn |first7=Michael S. |last8=Chan |first8=Bun |last9=Radom |first9=Leo |title=Preparation of an ion with the highest calculated proton affinity: ortho-diethynylbenzene dianion |journal=Chemical Science |date=2016 |volume=7 |issue=9 |pages=6245–6250 |doi=10.1039/C6SC01726F |pmid=30034765 |pmc=6024202 |doi-access=free}}

{{chem2|LiO−}} has a proton affinity of ~1782 kJ/mol.{{Cite journal|date=6 February 2016|doi=10.1016/j.cplett.2016.02.010|title=OLi3O anion: Designing the strongest base to date using OLi3 superalkali|last1=Srivastava|first1=Ambrish Kumar|last2=Misra|first2=Neeraj|journal=Chemical Physics Letters|volume=648|pages=152–155|bibcode=2016CPL...648..152S}}

Synthesis of the lithium monoxide anion

The anion is prepared in a mass spectrometer by successive decarboxylation and decarbonylation of lithium oxalate anion under collision-induced dissociation (CID) conditions:

:{{chem2|LiO\sC(\dO)\sCO2− → LiO\sC(\dO)− + CO2}}

:{{chem2|LiO\sC(\dO)− → LiO− + CO}}

The above method to synthesize the lithium monoxide anion is inefficient and difficult to carry out. The required ion rapidly reacts with traces of moisture and molecular oxygen present in the air. The reaction is further intensified by the high pressure argon that is introduced into the instrument to carry out the CID step.{{Cite journal|last1=Tian|first1=Zhixin|last2=Chan|first2=Bun|last3=Sullivan|first3=Michael B.|last4=Radom|first4=Leo|last5=Kass|first5=Steven R.|date=2008-06-03|title=Lithium monoxide anion: A ground-state triplet with the strongest base to date|journal=Proceedings of the National Academy of Sciences of the United States of America|volume=105|issue=22|pages=7647–7651|doi=10.1073/pnas.0801393105|issn=0027-8424|pmc=2409378|pmid=18511563|bibcode=2008PNAS..105.7647T|doi-access=free}}

References

{{Reflist}}

See also