Jump to content

Methine group: Difference between revisions

From Wikipedia, the free encyclopedia
Content deleted Content added
I changed it to enroll the way if sound be
sorry!
Line 10: Line 10:
</ref>
</ref>


==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.


Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.

==See also==
* [[Methyl group]] −{{chem|CH|3}}
* [[Methylene group]] or methylidene ={{chem|CH|2}}
* [[Methylene bridge]] or methanediyl −{{chem|CH|2}}−
* [[Methanetriyl group]] >CH−
* [[Methylylidyne group]] ≡C−

==References==
{{reflist}}

[[Category:Functional groups]]
[[Category:Substituents]]

{{Functional Groups}}
[[Image:Methine.svg|100px|right|thumb|Methine or methylylidene (IUPAC)]]
In chemistry, a '''methine group''' or '''methine bridge''' is a trivalent [[functional group]] =CH−, derived formally from [[methane]]. It consists of a [[carbon]] atom bound by two single [[covalent bond|bond]]s and one double bond, where one of the single bonds is to a [[hydrogen]]. The group is also called '''methyne''' or '''methene'''; its [[International Union of Pure and Applied Chemistry|IUPAC systematic name]] is '''methylylidene''' or '''methanylylidene'''<ref name=chebi>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;459B480BAF25AAC3CD9F2B5C3C3A9A07?chebiId=CHEBI:29432 ''Methanylylidene group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

This group is sometimes called "methylidyne", however that name belongs properly to either the [[methylidyne group]] ≡CH (connected to the rest of the molecule by a triple bond) or to the [[methylidyne radical]] '''⫶'''CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single [[covalent bond|bonds]], where one bond is to a [[hydrogen]] (>CH−).<ref name=chebi_2>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.


Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.
Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.
Line 73: Line 38:
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>
</ref>

==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.

Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.

==See also==
* [[Methyl group]] −{{chem|CH|3}}
* [[Methylene group]] or methylidene ={{chem|CH|2}}
* [[Methylene bridge]] or methanediyl −{{chem|CH|2}}−
* [[Methanetriyl group]] >CH−
* [[Methylylidyne group]] ≡C−

==References==
{{reflist}}

[[Category:Functional groups]]
[[Category:Substituents]]

{{Functional Groups}}
[[Image:Methine.svg|100px|right|thumb|Methine or methylylidene (IUPAC)]]
In chemistry, a '''methine group''' or '''methine bridge''' is a trivalent [[functional group]] =CH−, derived formally from [[methane]]. It consists of a [[carbon]] atom bound by two single [[covalent bond|bond]]s and one double bond, where one of the single bonds is to a [[hydrogen]]. The group is also called '''methyne''' or '''methene'''; its [[International Union of Pure and Applied Chemistry|IUPAC systematic name]] is '''methylylidene''' or '''methanylylidene'''<ref name=chebi>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;459B480BAF25AAC3CD9F2B5C3C3A9A07?chebiId=CHEBI:29432 ''Methanylylidene group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

This group is sometimes called "methylidyne", however that name belongs properly to either the [[methylidyne group]] ≡CH (connected to the rest of the molecule by a triple bond) or to the [[methylidyne radical]] '''⫶'''CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single [[covalent bond|bonds]], where one bond is to a [[hydrogen]] (>CH−).<ref name=chebi_2>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.

Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.

==See also==
* [[Methyl group]] −{{chem|CH|3}}
* [[Methylene group]] or methylidene ={{chem|CH|2}}
* [[Methylene bridge]] or methanediyl −{{chem|CH|2}}−
* [[Methanetriyl group]] >CH−
* [[Methylylidyne group]] ≡C−

==References==
{{reflist}}

[[Category:Functional groups]]
[[Category:Substituents]]

{{Functional Groups}}
[[Image:Methine.svg|100px|right|thumb|Methine or methylylidene (IUPAC)]]
In chemistry, a '''methine group''' or '''methine bridge''' is a trivalent [[functional group]] =CH−, derived formally from [[methane]]. It consists of a [[carbon]] atom bound by two single [[covalent bond|bond]]s and one double bond, where one of the single bonds is to a [[hydrogen]]. The group is also called '''methyne''' or '''methene'''; its [[International Union of Pure and Applied Chemistry|IUPAC systematic name]] is '''methylylidene''' or '''methanylylidene'''<ref name=chebi>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;459B480BAF25AAC3CD9F2B5C3C3A9A07?chebiId=CHEBI:29432 ''Methanylylidene group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

This group is sometimes called "methylidyne", however that name belongs properly to either the [[methylidyne group]] ≡CH (connected to the rest of the molecule by a triple bond) or to the [[methylidyne radical]] '''⫶'''CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single [[covalent bond|bonds]], where one bond is to a [[hydrogen]] (>CH−).<ref name=chebi_2>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.

Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.

==See also==
* [[Methyl group]] −{{chem|CH|3}}
* [[Methylene group]] or methylidene ={{chem|CH|2}}
* [[Methylene bridge]] or methanediyl −{{chem|CH|2}}−
* [[Methanetriyl group]] >CH−
* [[Methylylidyne group]] ≡C−

==References==
{{reflist}}

[[Category:Functional groups]]
[[Category:Substituents]]

{{Functional Groups}}
[[Image:Methine.svg|100px|right|thumb|Methine or methylylidene (IUPAC)]]
In chemistry, a '''methine group''' or '''methine bridge''' is a trivalent [[functional group]] =CH−, derived formally from [[methane]]. It consists of a [[carbon]] atom bound by two single [[covalent bond|bond]]s and one double bond, where one of the single bonds is to a [[hydrogen]]. The group is also called '''methyne''' or '''methene'''; its [[International Union of Pure and Applied Chemistry|IUPAC systematic name]] is '''methylylidene''' or '''methanylylidene'''<ref name=chebi>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;459B480BAF25AAC3CD9F2B5C3C3A9A07?chebiId=CHEBI:29432 ''Methanylylidene group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

This group is sometimes called "methylidyne", however that name belongs properly to either the [[methylidyne group]] ≡CH (connected to the rest of the molecule by a triple bond) or to the [[methylidyne radical]] '''⫶'''CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single [[covalent bond|bonds]], where one bond is to a [[hydrogen]] (>CH−).<ref name=chebi_2>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.

Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.

==See also==
* [[Methyl group]] −{{chem|CH|3}}
* [[Methylene group]] or methylidene ={{chem|CH|2}}
* [[Methylene bridge]] or methanediyl −{{chem|CH|2}}−
* [[Methanetriyl group]] >CH−
* [[Methylylidyne group]] ≡C−

==References==
{{reflist}}

[[Category:Functional groups]]
[[Category:Substituents]]

{{Functional Groups}}
[[Image:Methine.svg|100px|right|thumb|Methine or methylylidene (IUPAC)]]
In chemistry, a '''methine group''' or '''methine bridge''' is a trivalent [[functional group]] =CH−, derived formally from [[methane]]. It consists of a [[carbon]] atom bound by two single [[covalent bond|bond]]s and one double bond, where one of the single bonds is to a [[hydrogen]]. The group is also called '''methyne''' or '''methene'''; its [[International Union of Pure and Applied Chemistry|IUPAC systematic name]] is '''methylylidene''' or '''methanylylidene'''<ref name=chebi>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;459B480BAF25AAC3CD9F2B5C3C3A9A07?chebiId=CHEBI:29432 ''Methanylylidene group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

This group is sometimes called "methylidyne", however that name belongs properly to either the [[methylidyne group]] ≡CH (connected to the rest of the molecule by a triple bond) or to the [[methylidyne radical]] '''⫶'''CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single [[covalent bond|bonds]], where one bond is to a [[hydrogen]] (>CH−).<ref name=chebi_2>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.

Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.

==See also==
* [[Methyl group]] −{{chem|CH|3}}
* [[Methylene group]] or methylidene ={{chem|CH|2}}
* [[Methylene bridge]] or methanediyl −{{chem|CH|2}}−
* [[Methanetriyl group]] >CH−
* [[Methylylidyne group]] ≡C−

==References==
{{reflist}}

[[Category:Functional groups]]
[[Category:Substituents]]

{{Functional Groups}}
[[Image:Methine.svg|100px|right|thumb|Methine or methylylidene (IUPAC)]]
In chemistry, a '''methine group''' or '''methine bridge''' is a trivalent [[functional group]] =CH−, derived formally from [[methane]]. It consists of a [[carbon]] atom bound by two single [[covalent bond|bond]]s and one double bond, where one of the single bonds is to a [[hydrogen]]. The group is also called '''methyne''' or '''methene'''; its [[International Union of Pure and Applied Chemistry|IUPAC systematic name]] is '''methylylidene''' or '''methanylylidene'''<ref name=chebi>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;459B480BAF25AAC3CD9F2B5C3C3A9A07?chebiId=CHEBI:29432 ''Methanylylidene group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

This group is sometimes called "methylidyne", however that name belongs properly to either the [[methylidyne group]] ≡CH (connected to the rest of the molecule by a triple bond) or to the [[methylidyne radical]] '''⫶'''CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single [[covalent bond|bonds]], where one bond is to a [[hydrogen]] (>CH−).<ref name=chebi_2>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.

Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.

==See also==
* [[Methyl group]] −{{chem|CH|3}}
* [[Methylene group]] or methylidene ={{chem|CH|2}}
* [[Methylene bridge]] or methanediyl −{{chem|CH|2}}−
* [[Methanetriyl group]] >CH−
* [[Methylylidyne group]] ≡C−

==References==
{{reflist}}

[[Category:Functional groups]]
[[Category:Substituents]]

{{Functional Groups}}
[[Image:Methine.svg|100px|right|thumb|Methine or methylylidene (IUPAC)]]
In chemistry, a '''methine group''' or '''methine bridge''' is a trivalent [[functional group]] =CH−, derived formally from [[methane]]. It consists of a [[carbon]] atom bound by two single [[covalent bond|bond]]s and one double bond, where one of the single bonds is to a [[hydrogen]]. The group is also called '''methyne''' or '''methene'''; its [[International Union of Pure and Applied Chemistry|IUPAC systematic name]] is '''methylylidene''' or '''methanylylidene'''<ref name=chebi>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;459B480BAF25AAC3CD9F2B5C3C3A9A07?chebiId=CHEBI:29432 ''Methanylylidene group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

This group is sometimes called "methylidyne", however that name belongs properly to either the [[methylidyne group]] ≡CH (connected to the rest of the molecule by a triple bond) or to the [[methylidyne radical]] '''⫶'''CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single [[covalent bond|bonds]], where one bond is to a [[hydrogen]] (>CH−).<ref name=chebi_2>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.

Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.

==See also==
* [[Methyl group]] −{{chem|CH|3}}
* [[Methylene group]] or methylidene ={{chem|CH|2}}
* [[Methylene bridge]] or methanediyl −{{chem|CH|2}}−
* [[Methanetriyl group]] >CH−
* [[Methylylidyne group]] ≡C−

==References==
{{reflist}}

[[Category:Functional groups]]
[[Category:Substituents]]

{{Functional Groups}}
[[Image:Methine.svg|100px|right|thumb|Methine or methylylidene (IUPAC)]]
In chemistry, a '''methine group''' or '''methine bridge''' is a trivalent [[functional group]] =CH−, derived formally from [[methane]]. It consists of a [[carbon]] atom bound by two single [[covalent bond|bond]]s and one double bond, where one of the single bonds is to a [[hydrogen]]. The group is also called '''methyne''' or '''methene'''; its [[International Union of Pure and Applied Chemistry|IUPAC systematic name]] is '''methylylidene''' or '''methanylylidene'''<ref name=chebi>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;459B480BAF25AAC3CD9F2B5C3C3A9A07?chebiId=CHEBI:29432 ''Methanylylidene group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

This group is sometimes called "methylidyne", however that name belongs properly to either the [[methylidyne group]] ≡CH (connected to the rest of the molecule by a triple bond) or to the [[methylidyne radical]] '''⫶'''CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single [[covalent bond|bonds]], where one bond is to a [[hydrogen]] (>CH−).<ref name=chebi_2>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.

Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.

==See also==
* [[Methyl group]] −{{chem|CH|3}}
* [[Methylene group]] or methylidene ={{chem|CH|2}}
* [[Methylene bridge]] or methanediyl −{{chem|CH|2}}−
* [[Methanetriyl group]] >CH−
* [[Methylylidyne group]] ≡C−

==References==
{{reflist}}

[[Category:Functional groups]]
[[Category:Substituents]]

{{Functional Groups}}
[[Image:Methine.svg|100px|right|thumb|Methine or methylylidene (IUPAC)]]
In chemistry, a '''methine group''' or '''methine bridge''' is a trivalent [[functional group]] =CH−, derived formally from [[methane]]. It consists of a [[carbon]] atom bound by two single [[covalent bond|bond]]s and one double bond, where one of the single bonds is to a [[hydrogen]]. The group is also called '''methyne''' or '''methene'''; its [[International Union of Pure and Applied Chemistry|IUPAC systematic name]] is '''methylylidene''' or '''methanylylidene'''<ref name=chebi>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;459B480BAF25AAC3CD9F2B5C3C3A9A07?chebiId=CHEBI:29432 ''Methanylylidene group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

This group is sometimes called "methylidyne", however that name belongs properly to either the [[methylidyne group]] ≡CH (connected to the rest of the molecule by a triple bond) or to the [[methylidyne radical]] '''⫶'''CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single [[covalent bond|bonds]], where one bond is to a [[hydrogen]] (>CH−).<ref name=chebi_2>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.

Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.

==See also==
* [[Methyl group]] −{{chem|CH|3}}
* [[Methylene group]] or methylidene ={{chem|CH|2}}
* [[Methylene bridge]] or methanediyl −{{chem|CH|2}}−
* [[Methanetriyl group]] >CH−
* [[Methylylidyne group]] ≡C−

==References==
{{reflist}}

[[Category:Functional groups]]
[[Category:Substituents]]

{{Functional Groups}}
[[Image:Methine.svg|100px|right|thumb|Methine or methylylidene (IUPAC)]]
In chemistry, a '''methine group''' or '''methine bridge''' is a trivalent [[functional group]] =CH−, derived formally from [[methane]]. It consists of a [[carbon]] atom bound by two single [[covalent bond|bond]]s and one double bond, where one of the single bonds is to a [[hydrogen]]. The group is also called '''methyne''' or '''methene'''; its [[International Union of Pure and Applied Chemistry|IUPAC systematic name]] is '''methylylidene''' or '''methanylylidene'''<ref name=chebi>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;459B480BAF25AAC3CD9F2B5C3C3A9A07?chebiId=CHEBI:29432 ''Methanylylidene group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

This group is sometimes called "methylidyne", however that name belongs properly to either the [[methylidyne group]] ≡CH (connected to the rest of the molecule by a triple bond) or to the [[methylidyne radical]] '''⫶'''CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single [[covalent bond|bonds]], where one bond is to a [[hydrogen]] (>CH−).<ref name=chebi_2>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.

Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.

==See also==
* [[Methyl group]] −{{chem|CH|3}}
* [[Methylene group]] or methylidene ={{chem|CH|2}}
* [[Methylene bridge]] or methanediyl −{{chem|CH|2}}−
* [[Methanetriyl group]] >CH−
* [[Methylylidyne group]] ≡C−

==References==
{{reflist}}

[[Category:Functional groups]]
[[Category:Substituents]]

{{Functional Groups}}
[[Image:Methine.svg|100px|right|thumb|Methine or methylylidene (IUPAC)]]
In chemistry, a '''methine group''' or '''methine bridge''' is a trivalent [[functional group]] =CH−, derived formally from [[methane]]. It consists of a [[carbon]] atom bound by two single [[covalent bond|bond]]s and one double bond, where one of the single bonds is to a [[hydrogen]]. The group is also called '''methyne''' or '''methene'''; its [[International Union of Pure and Applied Chemistry|IUPAC systematic name]] is '''methylylidene''' or '''methanylylidene'''<ref name=chebi>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;459B480BAF25AAC3CD9F2B5C3C3A9A07?chebiId=CHEBI:29432 ''Methanylylidene group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

This group is sometimes called "methylidyne", however that name belongs properly to either the [[methylidyne group]] ≡CH (connected to the rest of the molecule by a triple bond) or to the [[methylidyne radical]] '''⫶'''CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single [[covalent bond|bonds]], where one bond is to a [[hydrogen]] (>CH−).<ref name=chebi_2>
(2007) [http://www.ebi.ac.uk/chebi/searchId.do;58A938AD0980FE8C9FAC6FF7D03B7F51?chebiId=CHEBI:29433 ''Methanetriyl group''] in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
</ref>

==Overlapping methines==
Two or more methine bridges can overlap, forming a chain or ring of carbon atoms connected by alternating single and double bonds, as in [[piperylene]] {{chem2|H2C\dCH\sCH\dCH\sCH3}}, or the compound
[[Image:Methine chain.svg|300px|center]]
Every carbon in this molecule is a methine carbon, except for three; two that are attached to the two [[nitrogen]]s and not to any hydrogens, and the one attached to the nitrogen, which is attached to two hydrogens (far right). There is a five carbon poly-methine chain in the center of this molecule.

Chains of alternating single and double bonds often form [[conjugated system]]s. When closed, as in [[benzene]] {{chem2|(\dCH\sCH\d)3}}, they often give [[aromatic (chemistry)|aromatic]] character to the compound.

==See also==
* [[Methyl group]] −{{chem|CH|3}}
* [[Methylene group]] or methylidene ={{chem|CH|2}}
* [[Methylene bridge]] or methanediyl −{{chem|CH|2}}−
* [[Methanetriyl group]] >CH−
* [[Methylylidyne group]] ≡C−

==References==
{{reflist}}

[[Category:Functional groups]]
[[Category:Substituents]]

{{Functional Groups}}

Revision as of 17:52, 6 November 2019

Methine or methylylidene (IUPAC)

In chemistry, a methine group or methine bridge is a trivalent functional group =CH−, derived formally from methane. It consists of a carbon atom bound by two single bonds and one double bond, where one of the single bonds is to a hydrogen. The group is also called methyne or methene; its IUPAC systematic name is methylylidene or methanylylidene[1]

This group is sometimes called "methylidyne", however that name belongs properly to either the methylidyne group ≡CH (connected to the rest of the molecule by a triple bond) or to the methylidyne radical CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single bonds, where one bond is to a hydrogen (>CH−).[2]


Chains of alternating single and double bonds often form conjugated systems. When closed, as in benzene (=CH−CH=)3, they often give aromatic character to the compound.

See also

References

  1. ^ (2007) Methanylylidene group in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
  2. ^ (2007) Methanetriyl group in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
Methine or methylylidene (IUPAC)

In chemistry, a methine group or methine bridge is a trivalent functional group =CH−, derived formally from methane. It consists of a carbon atom bound by two single bonds and one double bond, where one of the single bonds is to a hydrogen. The group is also called methyne or methene; its IUPAC systematic name is methylylidene or methanylylidene[1]

This group is sometimes called "methylidyne", however that name belongs properly to either the methylidyne group ≡CH (connected to the rest of the molecule by a triple bond) or to the methylidyne radical CH (the two atoms as a free molecule with dangling bonds).

The name "methine" is also widely used in non-systematic nomenclature for the methanetriyl group (IUPAC): a carbon with four single bonds, where one bond is to a hydrogen (>CH−).[2]

  1. ^ (2007) Methanylylidene group in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.
  2. ^ (2007) Methanetriyl group in the Chemical Entities of Biological Interest (ChEBI) database. Accessed on 2015-03-05.