IUPAC Gold Book - Sum Formulas

21/11/2017 IUPAC Gold Book - Sum formulas
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Indexes
Sum formulas
alphabetical
chemistry Exact chemical meaning
math/physics Ag Ag pH
general Ag solute-volatilization
interference in flame
source documents spectroscopy
Download Ag+ interfering substance
in electroanalytical
Gold Book PDF chemistry
AgBr AgBr molecular
rearrangement
FAQ AgCl AgCl pH
AgCl gravimetric method
about
AgI -AgI polymorphic transition
sitemap AgI crystalline electrodes
-AgI polymorphic transition
AgNO3 AgNO3 gravimetric method
Ag2S Ag2S crystalline electrodes
Al Al solute-volatilization
spectroscopy
AlCl3 AlCl3 ionization
AlNb3 Nb3Al superconducting
transition
Al2 2Al3+ mean activity of an
electrolyte in solution
Al2MgO4 MgAl2O4 solute-volatilization
spectroscopy
Ar Ar+ diamond by CVD
Ar gas-filled phototube
Ar excimer lamp
Ar+ diamond-like carbon
films
Ar cryogenic sampling
Ar Penning gas mixture
ArHOSe ArSeOH selenenic acids
Ar2 Ar2 excimer lamp

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As As photoconductive
detector
As poison in catalysis
AsF5 AsF5 dopant
AsH2 H2As+ arsanylium ions
AsH2O H2As(=O)+ arsanylium ions
AsH2O2 HAs(OH)2 arsonous acids
AsH3 AsH3 arsines
AsH3 arsanes
AsH3O H2AsOH arsinous acids
H3As=O arsine oxides
AsH3O2 AsH3O2 arsinic acids
AsH3O3 AsH3O3 arsonic acids
AsH4 (H4As+) onium compounds
AsH5 AsH5 arsoranes
As3H5 H2AsAsHAsH2 arsanes
As3H11 H4AsAsH3AsH4 arsanes
Au Au disproportionation
197
Au nuclear quadrupole
moment
(spectroscopic)
AuFe AuFe spin-glass transition
B B organically modified
silica
BH HB+ heteroconjugation
HB: carbene analogues
BH6N H3N BH3 dative bond
BN N B dative bond
B2BaO4 BaB2O4 optical parametric
oscillator
B2H BHB electron-deficient bond
B2H6 B2H6 electron-deficient bond
B5H9 B5H9 boranes
Ba Ba2+ mean activity of an
BaO3Ti BaTiO3 ferroelectric
(antiferroelectric)
transition
BiH3 BiH3 bismuthines
BiH3 bismuthanes
BiH4 (H4Bi+) onium compounds
Br Br excimer lamp
Br sulfonium compounds
Br addition reaction
Br telomerization
Br fragmentation
Br molecular
rearrangement
Br allylic substitution
reaction
Br leaving group
Br+ halonium ions
BrH BrH leaving group
BrH2 (H2Br+) onium compounds
BrKr KrBr excimer lamp
BrXe XeBr excimer lamp
C C multiply labelled
C transferases
C strain energy
C= heteroarenes
C organically modified
silica
13
C chemical shift, in
NMR
C potential-energy
(reaction) surface
C tautomerism
C dipolar compounds
C methylotrophic
microorganisms
C hydrogen bond in
theoretical organic
chemistry
C repulsive potential-
energy surface
12
C relative micellar mass
12
C molecular ion in mass
spectrometry
C spin polarization
CB BC potential-energy
(reaction) surface
BC repulsive potential-
energy surface
CBrCl3 CBrCl3 telomerization
CBr4 CBr4 rotator phase
transition
CCaO3 CaCO3 monotropic transition
CCl CCl coordination
CClF3 CF3Cl background
concentration (level) in
atmospheric chemistry
CCl2 :CCl2 carbenes
CCl2 -addition (alpha-
addition)
CCl2F2 CF2Cl2 background
concentration (level) in
CCl3 carbanion
Cl3C
CCl3 telomerization
telomerization
Cl3C.
chain transfer
Cl3C.
CF CF negative hyper-
conjugation
CH CH strain energy
CH agostic
CH symbiosis
CH steric isotope effect
HC carbynes
CH bicycle-pedal (BP)
mechanism
CH hypercoordination
CH persistent
CH= dipyrrins
CH carbaboranes
CH= quinones
CH , (sigma, pi)
CHN HCN isocyanides
HN+C isocyanides
C=NH imines
HCN nitriles
HCN cyanides
CHNO HOCN isocyanates
HN=C=O isocyanates
HON=C: fulminates
HCN+O fulminates
HOCN cyanates
CHNS HSCN thiocyanates
CHNSe HSeCN selenocyanates
CHO CHO characteristic group in
organic nomenclature
CHO2 COOH characteristic group in
COOH polyacid
CH2 CH2 strain energy
H2C silylene
CH2 insertion
:CH2 carbenes
H2C: carbenes
CH2 homoconjugation
CH2 meso structures in
polymers
carbynium ions
H2C.+
carbene radical
H2C.+
cations
CH2 tropyl radicals

CH2 hypercoordination
CH2 pyrromethenes
CH2 tropylium ions
H2C: alkylidenes
CH2 hydrocarbylene groups
CH2Cl ClCH2 organyl groups
CH2N2 CH2=N2 diazo compounds
HN=C=NH carbodiimides
CH2=N=N isoelectronic
CH2Na2O4 Na2CO310H2O efflorescence
CH2O CHOH oxo compounds
CHOH prochirality
CH2O fragmentation
CH2O smog chamber in
CH3 CH3 allylic intermediates
CH3 dimerization
CH3 colligation
CH3 bond-dissociation
energy,
CH3+ even-electron ion
CH3 strain energy
CH3 fragmentation
CH3 chain reaction
.CH radical (free radical)
3
CH3 benzylic intermediates

2
CH3( A'2) isogyric reaction
CH3 abstraction
CH3 , (sigma, pi)
CH3Cl CH3Cl molecular
rearrangement
CH3Cl substitution reaction
CH3ClO2S CH3ClO2S acyl halides
CH3F CH3F molecular laser
CH3I CH3I identity reaction
CH3IMg MeMgI organometallic
compounds
CH3N CH3N: carbene analogues
CH3N: nitrenes
CH3NO2 CH3NO2 azinic acids
CH3NO2 carbamates
CH3NO2S CH3N=S(=O)2 sulfonylamines
CH3NaS CH3SNa+ thiolates
CH3O CH2OH uronic acids
CH3O+ oxylium ions

OCH3 -electron
acceptor/donor group
CH3S CH3S sulfenyl groups
CH3S+ sulfenylium ions
MeS organyl groups
sulfenyl radicals
CH3S.
CH4 CH4 multiply labelled
CH4 reduced species
CH4 molecular entity
CH4 stoichiometry
CH4 bond energy (mean
bond energy)
CH4 composition of pure air
in atmospheric
chemistry
CH4(1A1) isogyric reaction
CH4 isotopologue
13
CH4+ isotope pattern in
mass spectrometry
CH4 isotope pattern in
mass spectrometry
12
CH4+ isotope pattern in
mass spectrometry
CH4 spectator mechanism
CH4 symbiosis
CH4 bond-dissociation
energy,
CH4 abstraction
CH4FN CH4FN negative hyper-
conjugation
CH4N2O CH4N2O isoureas
CH4N4 H2NN=CHN=NH formazans
CH4O CH3OH Brnsted acid
(CH3OH ) 2+
lyonium ion
CH4O substitution reaction
CH4O line formula
CH4O oxidative coupling
CH4O -addition (alpha-
addition)
CH3OH amphiprotic (solvent)
CH4O4 C(OH)4 ortho acids
CH4Si H2Si=CH2 heteroalkenes
CH5 CH5+ coordination number
+CH alkanium ions
5
CH5B CH5B spectator mechanism

CH5N3O NH2NHC(=O)NH2 semicarbazones
CH5P CH3PH2 phosphines

CIN ICN pseudohalogens
CKN KCN order-disorder
transition
CKNO KOCN cyanates
CN CN apicophilicity
CN interfering substance
chemistry
CN characteristic group in
CN lyases
CN prochirality
CN order-disorder
transition
CN pseudohalogens
CN carbonitriles
CN hydrolases
CN ligases (synthetases)
CNNa NaCN cyanides
CNNaO Na+[CN+O] fulminates
CNO NCO characteristic group in
CNS NCS organoheteryl groups
SCN pseudohalogens
CNS2 (SCN)2 pseudohalogens
CO C=O carbonyl compounds
C=O oxo compounds
CO photodecarbonylation
CO isoelectronic
CO oxocarbons
CO air pollutant
CO lyases
CO hydrolases
CO ligases (synthetases)
C(=O) quinones
CO2 CO2 sublimation
CO2 laser
CO2 reduced species
CO2 photodecarboxylation
CO2 photophosphorylation
CO2 molecular laser
CO2 composition of pure air
in atmospheric
chemistry
O=C=O heterocumulenes
CO2 acid rain in
O=C=O oxocarbons
CO2 cryogenic sampling

CO2 sanitary land fill
CO2 photosynthesis
CO2 greenhouse effect in
CO2 carbon dioxide laser
(CO2 laser)
CS CS ligases (synthetases)
CY CY bisecting conformation
(eclipsing
conformation)
C2 CC lyases
CC eclipsing strain
CC orbital symmetry
CC hydrolases
CC ligases (synthetases)
CC photohydration
CC symbiosis
C2H HCC carbanion
C2HNa NaCCH acetylides
C2H2 H2C=C: carbenes
H2C=C: vinylidenes
CH=CH heteroarenes
C2H2 flow rate in flame
emission and
absorption
spectrometry
C2H2 local fraction
atomized, , in
flame emission and
absorption
spectrometry
C2H2O CH2=C=O heterocumulenes
CH2=C=O isoelectronic
C2H3 CH2=CH vinylic groups
C2H3AgO2 C2H3AgO2 molecular
rearrangement
C2H3Cl C2H3Cl isodesmic reaction
:ClCH=CH2 conjugated system
(conjugation)
C2H3ClO C2H3ClO acyl halides
C2H3Cl3 C2H3Cl3 isodesmic reaction
C2H3N CH3CN cyanides
C2H3NS CH3SCN thiocyanates
C2H3O CH3C(=O) organyl groups
C2H3O2 CH2CO2H prochirality
C2H3O2 ionization
C2H3O2 proton transfer
reaction
CH3CO2 Brnsted base

C2H3O2 nucleophilic catalysis
C2H4 C2H4 disproportionation
C2H4 de Mayo reaction
C2H4 isodesmic reaction
C2H4 attachment
CH2CH2 meso structures in
polymers
C2H4 ene reaction
C2H4 sorptive insertion in
surface catalysis
+CH
2+CH2 dicarbenium ions
C2H4 hydration
C2H4 reactive adsorption
C2H4 negative hyper-
conjugation
C2H4 hyperconjugation
C2H4 sudden polarization
C2H4Cl2 C2H4Cl2 isodesmic reaction
C2H4Cl2NO C2H4Cl2NO aminoxyl radicals
nitroxides
(ClCH2)2NO.
C2H4Cl2O C2H4Cl2O -addition (alpha-
addition)
C2H4Cl3Pt [PtCl3(CH2=CH2)] chelation
C2H4F C2H4F negative hyper-
conjugation
C2H4F hyperconjugation
C2H4N iminyl radicals
CH3CH=N.
C2H4O C2H4O stoichiometry
C2H4O2 C2H4O2 ionization
CH3CO2H Brnsted acid
CH3CO2H prochirality
C2H4O2 proton transfer
reaction
C2H4O2 leaving group
C2H4O2 catalytic
hydrogenolysis
C2H4O3 CH3C(=O)OOH per acids
CH3C(=O)OOH peroxy acids
C2H5 CH3CH2+ carbenium ion
C2H5 disproportionation
CH3CH2 organyl groups
C2H5Br isotopic molecular ion
13
CCH5Br+.
isotopic molecular ion
13
C2H581Br+.
isotopic molecular ion

C2H581Br+.
C2H579Br molecular ion in mass
spectrometry
C2H5BrO BrCH2CH2OH halohydrins
C2H5Cl C2H5Cl nucleophile
(nucleophilic)
C2H5N MeN=CH2 heteroalkenes
C2H5NO2 H3N+CH2C(=O)O zwitterionic
compounds/zwitterions
C2H5N3O2 H2NNHC(=O)C(=O)NH2 semioxamazones
C2H6 C2H6 disproportionation
C2H6 catalytic
hydrogenolysis
C2H6 dimerization
C2H6 pseudorotation
CH313CH3 principal ion in mass
spectrometry
C2H6CuLi Li+[CuMe2] organometallic
compounds
C2H6NO C2H6NO aminoxides
C2H6N2 C2H6N2 carboxamidines
C2H6N2 isoelectronic
C2H6N4S2 H2NC(=NH)SSC(=NH)NH2 formamidine disulfides
C2H6O CH3CH[2H]OH singly labelled
CH3CH2OH constitutional
isomerism
CH3OCH3 constitutional
isomerism
CH3CH2OH prochirality
CH3CH2[18O][2H] mixed labelled
C2H6O hydration
C2H6O2 HOCH2CH2OH glycols
C2H6S MeCH2SH thiols
C2H7 [C2H7]+ alkanium ions
C2H7As CH3CH2AsH2 arsines
C2H7AsO2 C2H7AsO2 arsinic acids
C2H7NS CH3CH2SNH2 amides
C2H5SNH2 sulfenamides
C2H7S (CH3)2S+H onium compounds
C2H10O3Si3 C2H10O3Si3 cyclosiloxanes
C2N (CN)2 pseudohalogens
C3 C=C=C chirality axis
C3H2 c-(CH2)3 homodesmotic
reaction
C3H3AsO (CH3)3As=O arsine oxides
C3H3Bi (CH3)3Bi bismuthines
C3H3N CH2=CHCN conjugated system
(conjugation)
C3H4 H2C=CHCH: carbenes
H2C=CHC:H vinyl carbenes
C3H4O2 C3H4O2 de Mayo reaction
C3H5 H2C=CHCH2+ allylic intermediates
C3H5 delocalization
CH3CH2C alkylidynes
CH2=CHCH2 allylic groups
C3H5NO C3H5NO lactams
HOCH2CH2CN cyanohydrins
C3H5NO3 C3H5NO3 amic acids
C3H5NO3S C3H5NO3S imides
C3H5NSe CH3CH2SeCN selenocyanates
C3H5O C3H5O contributing structure
C3H5O abstraction
C3H6 +CH CH2+CH2 dicarbenium ions
2
radical ion
C3H6.+
C3H6 corrinoids
(cobalamines,
corphyrins, corrins,
vitamin B12
compounds)
diradicals
H2C.CH2C.H2
CH3CH2CH: alkylidenes
CH2CH2CH2 hydrocarbylene groups
C3H6 ene reaction
C3H6O C3H6O abstraction
C3H6O epoxy compounds
C3H6O proton transfer
reaction
C3H6O PaternoBchi
reaction
C3H6O isoelectronic
C3H6O fragmentation
C3H6O dimerization
C3H6S CH3CH2C(=S)H thioaldehydes
C3H7 CH3CH2CH2+ carbenium ion
alkyl radicals
CH3CH2C.H2
C3H7Br C3H7Br molecular
rearrangement
C3H7ClO ClCH2CH2CH2OH halohydrins
C3H7N EtCH=NH aldimines
C3H7O C3H7O fragmentation
C3H7O proton transfer
reaction
C3H8 C3H8 catalytic

hydrogenolysis
C3H8O2S (CH3)2CHS(=O)OH sulfinic acids
C2H5S(=O)2CH3 sulfones
C3H9ClP Cl(CH3)3P+ onium compounds
C3H9ClS [(CH3)3S]+Cl sulfonium compounds
C3H9N C3H9N ammoniumyl radical
ions
NMe3 leaving group
C3H9N leaving group
C3H9NO (CH3)3N+O zwitterionic
compounds/zwitterions
C3H9NO2S C3H9NO2S amides
C3O2 O=C=C=C=O heterocumulenes
O=C=C=C=O oxocarbons
C4H4 3 CH2=CH2 homodesmotic
reaction
C4H4N2 C4H4N2 pyrimidine bases
C4H4N2 heteroarenes
C4H4O2 HO[CH2]4OH glycols
C4H4O2 isolated double bonds
C4H4S C4H4S heteroarenes
C4H5N C4H5N indicated hydrogen
C4H5NO2 C4H5NO2 imides
C4H6 C4H6 attachment
C4H6 non-Kekul molecules
C4H6 addition reaction
trimethylenemethanes
CH2=C(C.H2)2
CH3CH=C=CH2 dienes
CH2=CHCH=CH2 dienes
CH2=CHCH=CH2 conjugated system
(conjugation)
3 CH3CH3 homodesmotic
reaction
C4H6 cheletropic reaction
C4H6 s-cis, s-trans
C4H6Br2 C4H6Br2 addition reaction
C4H6O C4H6O oxa-di--methane
rearrangement
C4H6O2S C4H6O2S cheletropic reaction
C4H6O3 C4H6O3 acid anhydrides
C4H6O4 C4H6O4 oxidative coupling
C4H6O6 C4H6O6 meso-compound
C4H7Br C4H7Br allylic substitution
reaction
C4H7ClO2Zn ClZnCH2C(=O)OEt organometallic
compounds
C4H7NO (CH3)2C(OH)CN cyanohydrins
C4H7Y C4H7Y chain polymerization
C4H8 C4H8 addition reaction
C4H8 cycloalkanes
C4H8 anti
C4H8Br2 C4H8Br2 anti
C4H8O C4H8O multiply labelled
CH3CH2COCH3 prochirality
C4H8O allylic substitution
reaction
C4H8S CH3C(=S)CH2CH3 thioketones
C4H9 C4H9 hyperconjugation
C4H9Br C4H9Br addition reaction
C4H9FO C4H9FO diastereotopic
C4H9N C4H9N pre-equilibrium (prior
equilibrium)
C4H10 C4H10 catalytic
hydrogenolysis
C4H10Mg Et2Mg organometallic
compounds
C4H10N C4H10N pre-equilibrium (prior
equilibrium)
CH3CH2OCH2CH3 ethers
CH3CH2CHOHCH3 prochirality
C4H10O diastereotopic
CH3CHOHCH2CH3 prochirality
C4H10O3 HC(OCH3)3 ortho esters
C4H11N ylides
(CH3)3N+CH2
C4H11NO C4H11NO pre-equilibrium (prior
equilibrium)
C4H11O3PS C4H11O3PS betaines
C4H12N2 C4H12N2 amine imides
C4H13NO [(CH3)4N]+OH quaternary ammonium
compounds
C4O4 C4O4 oxocarbons
C5 C5 terpenes
C5H3BrN4 C5H3BrN4 tele-substitution
C5H4 C5H4 nonclassical structure
C5H4 electrocyclic reaction
C5H4N2O C5H4N2O topomerization
C5H4N4 C5H4N4 purine bases
C5H5N C5H5N+ organoheteryl groups
C5H5N nucleophilic catalysis

C5H5NO C5H5NO tautomerism
C5H5NOS C5H5NOS penems
C5H5N5 C5H5N5 tele-substitution
C5H5OP C5H5OP indicated hydrogen
C5H5P C5H5P indicated hydrogen
C5H7NOS C5H7NOS penams
C5H7O2 C5H7O2 carbanion
C5H8 C5H8 di--methane
rearrangement
3 CH3CH2CH3 homodesmotic
reaction
C5H8 sigmatropic
rearrangement
[CH2=C(CH3)CH=CH2] terpenes
C5H8OS2 CH3C(=O)SC(=S)CH2CH3 thioanhydrides
C5H8O2 C5H8O2 de Mayo reaction
C5H8O3 HC(=O)CH2CH2CH2C(=O)OH oxo carboxylic acids
C5H8O5 HO2CCH2CHOHCH2CO2H prochirality
C5H8O7 C5H8O7 pseudo-asymmetric
carbon atom
C5H9Br C5H9Br molecular
rearrangement
C5H9N C5H9N aza-di--methane
rearrangement
C5H9NO2 C5H9NO2 imino acids
C5H9O C5H9O ambident
C5H10 C5H10 envelope conformation
C5H10 ene reaction
C5H10O C5H10O prochirality
C5H10O molecular
rearrangement
C5H10O2 C5H10O2 molecular
rearrangement
C5H10O4 C5H10O4 monosaccharides
C5H11NO2 C5H11NO2 betaines
C5H12 Me4C symbiosis
C5H12O4 C(OCH3)4 ortho esters
C5H12O5 C5H12O5 meso-compound
C5H14NO4P Me3N+CH2CH2OP(=O) phospho
(OH)O
C5H15Ta TaMe5 homoleptic
C6H4 C6H4 aryne
C6H4NS2 C6H4NS2 Herz compounds
C6H4O2 C6H4O2 quinones
C6H4O2 quinhydrones
C6H5 C6H5 aryl cations
C6H5AsCa CaAsPh arsenides

C6H5I C6H5I isotopic scrambling
C6H5KN2O PhN=NOK+ diazoates
C6H5NO2 C6H5NO2 electrophile
(electrophilic)
C6H5N2 C6H5N2 isotopic scrambling
PhN+N diazonium salts
C6H5N3 PhN3 azides
C6H5Y C6H5Y Hammett equation
(Hammett relation)
C6H6 C6H62+ nonclassical structure
C6H6 Kekul structure (for
aromatic compounds)
C6H6 electrophile
(electrophilic)
C6H6 catalytic
hydrogenolysis
C6H6 homodesmotic
reaction
3 CH2=CHCH=CH2 homodesmotic
reaction
C6H6 fulvenes
radical ion
C6H6.
radical ion
C6H6.+
C6H6NNa C6H6NNa anilides
C6H6N2 C6H6N2 quinonimines (quinone
imines)
C6H6N2O PhN=NOH diazoates
C6H6O C6H6O valence
tautomerization
C6H6O arene epoxides
C6H6OS PhSOH sulfenic acids
C6H6O2 C6H6O2 quinhydrones
C6H6O4 C6H6O4 cycloaddition
C6H6O4S PhS(=O)2OOH peroxy acids
C6H7 C6H7+ arenium ions
C6H7N C6H5NH2 transformation
C6H7N isotopic scrambling
C6H7N ammoniumyl radical
ions
C6H8 C6H8 electrocyclic reaction
C6H8NO2P C6H8NO2P amides
C6H8N2S PhS(=NH)NH2 sulfinamidines
C6H9Br C6H9Br anti
C6H9NOS C6H9NOS cephams
C6H9N3O2 C6H9N3O2 pros in histidine
nomenclature
C6H9Sb (CH2=CH)3Sb stibines

C6H10 C6H10 degenerate
rearrangement
C6H10 half-chair
C6H10 attachment
C6H10 carbenes
C6H10BrF C6H10BrF anti
C6H10Br2NiP2 Ni[(CH3)2PCH2CH2P(CH3)2]Br2 (kappa) in inorganic
nomenclature
C6H10O3 C6H10O3 tautomerism
C6H10O4 C6H10O4 enoses
C6H10O7 C6H10O7 uronic acids
C6H10O7 ketoaldonic acids
C6H11BrO5 C6H11BrO5 anomeric effect
C6H11NO C6H11NO prochirality
C6H11NO lactams
C6H11S C6H11S sulfonium compounds
C6H12 C6H12 oxidative addition
C6H12 chair, boat, twist
C6H12 PaternoBchi
reaction
C6H12 cyclo-
C6H12O2 C6H12O2 dimerization
C6H12O3 C6H12O3 acetonides
C6H12O5 C6H12O5 (alpha), (beta)
C6H12O6 C6H12O6 aldoses
C6H12O6 Haworth
representation
C6H12O6 ketoses
C6H12O6 (alpha), (beta)
C6H12O7 C6H12O7 aldonic acids
C6H12Si C6H12Si di--silane
rearrangement
C6H13NO5 C6H13NO5 amino sugars
C6H14 C6H14 cyclo-
C6H14LiN C6H14LiN amides
C6H14N C6H14N abstraction
C6H14O6 C6H14O6 Haworth
representation
C6H15B Et3B organometallic
compounds
C6H15N C6H15N abstraction
C6N4 C6N4 -adduct
C7H4ClO2 C7H4ClO2 isodesmic reaction
C7H4O3S2 C7H4O3S2 cyclic acid anhydrides
(cyclic anhydrides)
C7H5ClO2 C7H5ClO2 isodesmic reaction
C7H5NO PhOCN cyanates

C7H5O2 C7H5O2 isodesmic reaction
C7H6 C7H6 annulenylidenes
C7H6FeO2S [Fe(CO)3(C4H6SO)] (eta or hapto) in
inorganic
nomenclature
C7H6N C7H6N nitrilium ions
C7H6O C7H6O quinomethanes
C7H6O tropones
C7H6OS PhC(=S=O)H sulfines
C7H6O2 C7H6O2 isodesmic reaction
C7H6O2 tropolones
C7H7 C7H7 common-ion effect (on
rates)
C7H7 benzylic intermediates
(C7H72+) mass-to-charge ratio,
in mass
spectrometry
C7H7+ tropylium ions
C7H7Br C7H7Br leaving group
C7H7BrO C7H7BrO cine-substitution
C7H7Cl C7H7Cl common-ion effect (on
rates)
C7H7NO C7H7NO amides
C7H7NS PhC(=S)NH2 thio
C7H8 C7H8 cycloaddition
C7H8 catalytic
hydrogenolysis
C7H8 tropilidenes
C7H8 catalytic
dehydrocyclization
C7H8NO C7H8NO nucleophilic catalysis
C7H8O C7H8O common-ion effect (on
rates)
C7H9N C7H9N catalytic
hydrogenolysis
C7H9NO C7H9NO cine-substitution
C7H9NOS PhS(=O)NHCH3 sulfinamides
C7H9NO2S PhS(=O)2NHCH3 sulfonamides
C7H10BrF C7H10BrF endo, exo, syn, anti
C7H12 C7H12 anti
C7H12ClN C7H12ClN acyl halides
C7H14N2 C7H14N2 carboxamidines
C7H14O C7H14O Norrish Type II
photoreaction
C7H14O6 C7H14O6 anomeric effect

dehydrocyclization
C8H4O C8H4O heteroarynes
C8H5NO C8H5NO cyanides
C8H6CrO [Cr(CO)4(C4H6)] (eta or hapto) in
inorganic
nomenclature
C8H6S2 C8H6S2 isolated double bonds
C8H8 C8H8 chain reaction
C8H8 non-Kekul molecules
C8H8 chain transfer
C8H8 quinomethanes
C8H8 alternant
C8H8 polyhedranes
C8H8ClNO C8H8ClNO molecular
rearrangement
C8H8O4 C8H8O4 polyketides
C8H8O4S C8H8O4S acid anhydrides
C8H9 (C8H9+) homoaromatic
C8H9ClO PhCH(OH)CH2Cl halohydrins
C8H9N PhCH=NMe aldimines
C8H9NO C6H5NHCOCH3 transformation
C8H9NO molecular
rearrangement
C8H9NO anilides
C8H10S C8H10S leaving group

C8H11ClO C8H11ClO (alpha), (beta)
C8H11NOS (CH3)2S(=O)=NPh sulfoximides
C8H12 propellanes
C8H12N C8H12N aminium ions
C8H14 C8H14 planar chirality
C8H14O4 C8H14O4 monosaccharides
C8H16 C8H16 tub conformation
C8H16 crown conformation
C8H16 extrusion
transformation
C8H16N2 C8H16N2 extrusion
transformation
hydrogenolysis
C8H18O C8H18O zig-zag projection
C8H20N (CH3CH2)4N+ onium compounds
C8K C8K intercalation reaction
C9H5N C9H5N heteroarynes
C9H6O2 C9H6O2 isocoumarins

C9H6O2 coumarins
C9H8Cl3 C9H8Cl3 chain transfer
C9H8N2 C9H8N2 dipyrrins
C9H10O C9H10O molecular
rearrangement
C9H10O2 C9H10O2 leaving group
C9H10O2 catalytic
hydrogenolysis
C9H12 C9H12 -adduct
C9H12S (CH3)2S=CHPh ylides
(CH3)2S+CHPh ylides
C9H14 C9H14 Bredt's rule
C9H16 C9H16 spiro compounds
C9H16O2 C9H16O2 tritactic polymer
C9H18O C9H18O PaternoBchi
reaction
C9H19NO4 C9H19NO4 glycosylamines
C10 C10 monoterpenoids
C10 terpenes
C10H6 C10H6 dehydroarenes
C10H8 C10H8 fulvalenes
C10H8 alternant
C10H8O C10H8O phenols
C10H10 C10H10 non-Kekul molecules
C10H10 polyquinanes
(polyquinenes)
C10H14NO C10H14NO amidium ions
C10H15NS (C2H5)2S=NPh sulfimides
C10H16 ring assembly
C10H18 C10H18 cis-trans isomers
C10H20 C10H20 iridoids
C11H6O3 C11H6O3 furocoumarins
C11H12O4 C11H12O4 acylals
C11H14 C11H14 hula-twist (HT)
mechanism
C11H14 bicycle-pedal (BP)
mechanism
C12H8 C12H8 ring assembly
C12H8Cl2 C12H8Cl2 meso-compound
C12H10 C12H10 ring assembly
C12H10N2 PhN=NPh azo compounds
C12H10N2O C12H10N2O azoxy compounds
C12H10OS Ph2S=O sulfoxides
C12H10O5S2 PhS(=O)2OS(=O)2Ph sulfonic anhydrides

C12H12N2S Ph2S(=NH)2 sulfonediimines
C12H14 C12H14 anti
C12H24O6 C12H24O6 crown
C12O9 C12O9 oxocarbons
C13H10O radical ion
Ph2CO.
C13H12O2 C13H12O2 bisphenols
C13H13N3 PhN=NNPhMe diazoamino
compounds
C13H13OP (Ph)2POCH3 esters
C13H14 C13H14 spiro compounds
C13H14O4 C13H14O4 cycloaddition
C13H16O7 C13H16O7 glycosides
C14H10 C14H10 quinarenes
C14H10 acenes
C14H10O C14H10O epoxy compounds
C14H10OS2 C14H10OS2 acid anhydrides
C14H10O9 C14H10O9 depsides
C14H12 C14H12 cycloaddition
C14H12N6O3 C14H12N6O3 folates
C14H24 C14H24 propellanes
C15 C15 sesquiterpenoids
C15 terpenes
C15H10O2 C15H10O2 flavonoids
(isoflavonoids and
neoflavonoids)
C15H11O C15H11O anthocyanidins
C15H16N (p-Me2NC6H4)2CHPh leuco bases
C16H10 C16H10 ortho- and peri-fused
(polycyclic
compounds)
C16H14O PhC(=O)CH=C(CH3)Ph dypnones
C16H16 C16H16 cyclophanes
C17H16Cl3 C17H16Cl3 chain transfer
C17H21NO4 C17H21NO4 pseudo-asymmetric
carbon atom
C17H21N2 C17H21N2 cyanine dyes
C17H28 C17H28 steroids
C18H12 C18H12 ortho-fused (polycyclic
compounds)
C18H14 C18H14 quinarenes
C18H34O9 C18H34O9 in-out isomerism
C18H36N2O6 C18H36N2O6 cryptand
C19H12 C19H12 ortho- and peri-fused
(polycyclic
compounds)
C19H14N4 C19H14N4 tetrapyrroles
C19H14O5S C19H14O5S sulfonphthaleins

C19H15 C19H15 fragmentation
C19H16 C19H16 bicycle rearrangement
C19H17P Ph3P+CH2 ylides
Ph3P+=CH2 ylides
C19H22N4 C19H22N4 corrinoids
(cobalamines,
corphyrins, corrins,
vitamin B12
compounds)
C19H30 C19H30 cyclo-
C19H32 C19H32 cyclo-
C19H32 abeo-
C19H32 seco-
C19H32O C19H32O (alpha), (beta)
C19H34 C19H34 seco-
C20 C20 prostaglandins
C20 leukotrienes
C20 terpenes
C20 diterpenoids
C20 icosanoids
C20H12O5 C20H12O5 xanthene dyes

C20H14N4 C20H14N4 porphyrins
C20H14O4 C20H14O4 phthaleins
C20H16O2 C20H16O2 fragmentation
C20H19OP C20H19OP betaines
C20H20O5 C20H20O5 lignans
C20H38O2 C20H38O2 prostaglandins
C22H23ClN2O8 C22H23ClN2O8 tetracyclines
C22H26O6 C22H26O6 lignans
C23H22O6 C23H22O6 rotenoids
C25 C25 terpenes
C25 sesterterpenoids
C26H16 C26H16 helicenes
C26H16 helicity
C27H54N2 C27H54N2 in-out isomerism
C30 C30 terpenes
C30 triterpenoids
C30H42O C30H42O carotenoids
C38H24Cl4 C38H24Cl4 biradical
C40 C40 terpenes
C40 carotenoids
C40 tetraterpenoids
C40H56 C40H56 retro
C40H56 carotenoids
C40H56O2 C40H56O2 carotenoids

C41H29NO C41H29NO DimrothReichardt
parameter
Ca Ca2+ interfering substance
chemistry
Ca2+ selectivity coefficient,
in ion exchange
chromatography
Ca 2+
ionic conductivity
CaFeO3 CaFeO3 disproportionation
Cd Cd resonance lamp
CdHe HeCd ion laser
CdHgTe HgCdTe photoconductive
detector
CdS CdS pressure-induced
transition
CdS photoconductive
detector
Cl Cl abstraction
Cl pH
Cl apicophilicity
Cl characteristic group in
Cl gas sensing electrode
Cl nucleofuge
Cl Herz compounds
Cl chain reaction
Cl Brnsted base
Cl substitution reaction
chain reaction
Cl.
Cl excimer lamp
Cl selectivity coefficient,
in ion exchange
chromatography
Cl nucleophile
(nucleophilic)
radical (free radical)
Cl.
Cl common-ion effect (on
rates)
Cl+ halonium ions
Cl ionization
Cl gravimetric method
Cl photolysis
Cl conjugate acidbase
pair
ClCs CsCl thermally-induced
transition
CsCl structural transition

CsCl first-order phase
transition
CsCl dilational (dilatational)
transition
ClH HCl oxoacids
ClH reaction path
degeneracy
HCl Brnsted acid
ClH isotope exchange
ClH molecular
rearrangement
HCl levelling effect
ClH abstraction
HCl internal filling solution
of a glass electrode
HCl conjugate acidbase
pair
ClHO HOCl oxoacids
ClHO4 HClO4 levelling effect
ClH2 (H2Cl+) onium compounds
ClH4N NH4Cl structural transition

ClK KCl membrane emf
KCl Donnan emf (Donnan
potential)
ClKr KrCl excimer lamp
ClLiO4 LiClO4 special salt effect
ClNa NaCl pressure-induced
transition
NaCl thermally-induced
transition
NaCl structural transition
NaCl first-order phase
transition
ClXe XeCl excimer lamp
XeCl excimer laser
Cl2 Cl2 gas sensing electrode
Cl2 polarizability
2Cl mean activity of an
Cl2 excimer lamp
Cl2F (Cl2F+) onium compounds
Cl2Zn ZnCl2 activated carbon
Cl4Rb2Zn Rb2ZnCl4 commensurate
incommensurate
transition
Co Co3+ spin-state transition
CoLaO3 LaCoO3 spin-state transition
Cr Cr3+ solid state lasers
Cr3+ ruby laser

Cu Cu Penning gas mixture
CuI CuI chelation
CuMn CuMn spin-glass transition
CuZn CuZn second-order
transition
F F apicophilicity
F negative hyper-
conjugation
F hydrogen bond
F excimer lamp
F branching ratio
F+ halonium ions
F hyperconjugation
FH HF molecular laser
HF superacid
HF chemical laser
HF branching ratio
FHO3S HSO3F superacid
FH2
(H2F+) onium compounds
FKr KrF excimer laser
KrF liquid ion laser
F2P FapPFap hypervalency
F5P PF5 hypervalency
PF5 polytopal
rearrangement
F5Sb SbF5 superacid
F6S SF6 air mass in
F6U UF6 gaseous diffusion
separator in
Fe Fe3+ Verwey transition
Fe2+ Verwey transition
Fe exchange-inversion
transition
Fe3+ order-disorder
transition
Fe2+ Fenton reaction
Fe3+ Fenton reaction
57
Fe quadrupole splitting in
Mssbauer
spectroscopy
Fe3+ equivalent entity
Fe2+ oxidized species
Fe3+ oxidized species
Fe oxidized species
57
Fe nuclear quadrupole
moment
(spectroscopic)
Fe spin crossover
FeII spin crossover
FeIII salt form of an ion
exchanger
FeII salt form of an ion
exchanger
FeLiO2 LiFeO2 order-disorder
transition
FeMo MoFe spin-glass transition
FeRh FeRh exchange-inversion
transition
Fe2O3 -Fe2O3 Morin transition
Fe3O4 Fe3+[Fe3+Fe2+]O4 Verwey transition
H H hyperconjugation
H+ leaving group
H+ general acidbase
catalysis
H carbene analogues
H selenides
H bismuthines
H+ pH
H selenoxides
H oxime O-ethers
H+ extraction (equilibrium)
constant
H nucleophilic catalysis
H hydron
H+ hydron
H hydron
H multiply labelled
H+ gas sensing electrode
2
H deuterium
2
H deuterium
H+
2 deuterium
H tautomerism
H hydrogen
H selones
H+ electrofuge
H urethanes (urethans)
H extended Hammett
equation
H ketones
H ketoximes
H Schiff bases (Schiff's
bases)
H hemiketals
H sulfenyl radicals
H+ isoionic
H+ ligands
H+ catalytic coefficient
H hemiaminals
H stibines
H tellurides
H ethers
1
H chemical shift, in
NMR
2
H deuteron
H+ tautomerism
H thioethers
H dual substituent-
parameter equation
H azomethines
H thioketone S-oxides
H pseudo acids
H branching chain
reaction
H imines
1
H aromatic
3
H electron capture
detector in gas
chromatography
H alkyl groups
H esters
H sulfenylium ions
H trioxides
H electrophile
(electrophilic)
H+ protonation constant
H polysulfanes
H nitrones
H selenols
H+ Rutherford
backscattering (RBS)
H sulfenic acids
H+ specific acidbase
catalysis
H thioketones
H diazoamino
compounds
H bond energy (mean
bond energy)
H sulfenamides
H bond-dissociation
energy,
H+ equivalent entity
H silicones
H gas-phase acidity
H sulfenyl groups
H Hammett equation
(Hammett relation)
H sulfoxides
H gas-phase basicity
H polysulfides
H hydrazides
H enols
H alkoxyamines
H ortho esters
H phosphines
3
H+ tritium
3
H tritium
3
H tritium
1
H protium
1
H+ protium
H+ protium
H acetals
H selenenic acids
H+ HaberWeiss reaction
H arsines
H reaction path
degeneracy
H thiohemiacetals
H ketals
H fragmentation
H thioacetals
H sulfones
H(2S) isogyric reaction
H thiols
H addition reaction
H spin polarization
H hemiacetals
H Brnsted relation
H ketimines
H+ standard hydrogen
electrode
H sulfides
H common-ion effect (on
rates)
HI HI levelling effect
HLi HLi topochemical reaction
LiH oxidation state
HN NH anion exchanger
HN: carbene analogues
HN: nitrenes
NH silasesquiazanes
NH silazanes
HN Lewis acid
HN= imino acids
HNO =NOH hydroximic acids
HNO2 HON=O oxoacids
HONO smog chamber in
HNO3 HNO3 smog chamber in
HN3 N=NNH azimines
HN3 azides
HO OH anion exchanger
OH general acidbase
catalysis
OH vinylic groups
OH hydrazidines
HO allylic substitution
reaction
OH characteristic group in
OH erythro structures in a
polymer
OH isoionic
HO substitution reaction
OH catalytic coefficient
OH benzylic groups
OH phosphoglycerides
OH Fenton reaction
OH phosphoramides
HO anhydro bases
OH oxo compounds
OH cresols
OH kinetic equivalence
OH specific acidbase
catalysis
HO pre-equilibrium (prior
equilibrium)
OH allylic groups
HO+ oxylium ions
OH anilides
OH Brnsted base
OH sulfenamides
HO decay rate in
OH hydrazides
alcohols
HO.
OH alcohols
OH hydroxamic acids
HO molecular
rearrangement
HO acyl species
acyl species
HO.
HO+ acyl species
Fenton reaction
OH.
HaberWeiss reaction
OH.
OH HaberWeiss reaction
HO colligation
OH branching chain
reaction
HO smog chamber in
OH peroxy acids
HO2 OOH peroxy acids
HO3S SO3H characteristic group in
SO3H polyacid
HO4S HSO4 Brnsted acid
HSO4 Brnsted base
HSi SiH agostic
SiH silasesquiazanes
H2 H2 pH
H2 gas sensing electrode
H2 catalytic
hydrogenolysis
H2(1+g) isogyric reaction
H2 standard hydrogen
electrode
H2I (H2I+) onium compounds
H2KN H2KN isotopic scrambling
H2N NH2 amides
NH2 characteristic group in
NH2 phosphoglycerides
aminyl radicals
H2N.
(H2N:+) nitrenium ions
H2NO H2NO aminoxides
nitroxides
H2NO.
NHOH hydroxamic acids
H2NP HP=NH phosphazenes
H2N2 =NNH2 hydrazidines
H2NN: carbene analogues
NHNH hydrazo compounds
=NNH2 hydrazones
HN=NH azo compounds

H2N2O H2NNO nitrosamides
H2N2O2 O2NNH2 nitramines
H2N2S HN=S=NH sulfur diimides
H2O H2O oxenium ions
H2O common-ion effect (on
rates)
H2O ionization
H2O composition of pure air
in atmospheric
chemistry
H2O temperature lapse rate
in atmospheric
chemistry
H2O Brnsted acid
H2O supersaturation
H2O Brnsted base
H2O oxidative coupling
H2O nucleophilic catalysis
H2O anhydro bases
H2O hydration
H2O branching chain
reaction
H2O pre-equilibrium (prior
equilibrium)
H2O gaseous diffusion
separator in
H2O HaberWeiss reaction
H2O sanitary land fill
H2O photosynthesis
H2O amphiprotic (solvent)
H2O2 HOOH hydroperoxides
H2O2 Fenton reaction
H2O2 oxidation state
H2O2 HaberWeiss reaction
H2O2 smog chamber in
H2O2S HOSOH oxoacids
HS(=O)OH sulfinic acids
H2O3 HOOOH trioxides
H2O3P PO3H2 characteristic group in
P(=O)(OH)2 phospho
P(=O)(OH)2 phosphono
PO3H2 polyacid
H2O3S HS(=O)2OH sulfonic acids
H2O4S (HO)2SO2 oxoacids
H2SO4 reduced species

H2SO4 Brnsted acid
H2SO4 equivalent entity
H2SO4 oxidation state
H2SO4 haze in atmospheric
chemistry
H2SO4 amphoteric
H2S H2S hydrocracking unit
H2S reduced species
SH2 bonding number
H2S sulfenylium ions
H2S acid-labile sulfur
H2S oxidized species
H2S sulfenyl groups
H2S sulfenyl radicals
H2S oxidation state
H2S sulfanes
H2S air pollutant
H2S2 HS2H polysulfanes
H2Se H2Se selenides
H2Si H2Si: silylene
H2Si silylene
H2Te H2Te tellurides
H3N ammoniumyl radical
H3N.+
ions
H3N aminiumyl radical ions
NH3 Brnsted acid
NH3 Rydberg state
H3N tele-substitution
H3NO H2NOH hydroxylamines
H3NO2 H3NO2 azinic acids
H3NO3 H3NO3 azonic acids
H3NO3S H2NS(=O)2OH sulfamic acids
H3NS H2S=NH sulfimides
H3N2 NHNH2 hydrazidines
verdazyl radicals
H2NN.H
H3N3 NH2N=NH triazenes
H3O H3O+ oxonium ions
H3O ionization
H3O+ Brnsted acid
(H3O+) onium compounds

H3OP H2POH phosphinous acids
H3O2P HP(OH)2 phosphonous acids
H2P(=O)OH phosphinic acids
H3O3P P(OH)3 oxoacids

HP(=O)(OH)2 phosphonic acids
H3O4P H3PO4 electrolytic hygrometer
H3P PH3 phosphines
PH3 phosphanes
H3S (H3S+) onium compounds
H3Sb SbH3 stibanes
SbH3 stibines
H3Se (H3Se+) onium compounds
H3Si H3Si silyl groups
silyl radicals
H3Si.
H3Sn .SnH radical (free radical)
3
H3Te (H3Te+) onium compounds

H4N (H4N+) onium compounds
H4NP H3P=NH phosphazenes
H4NY (NH4+)Y quaternary ammonium
compounds
H4N2 H2NNH2 hydrazines
H4OSi H3SiOH silanols
H4P (H4P+) onium compounds
H4Sb (H4Sb+) onium compounds
H5NO4S NH4HSO4 haze in atmospheric
chemistry
H5N3 NH2NHNH2 triazanes
H5P PH5 phosphoranes
H6S SH6 bonding number
H10N2Si3 H3SiNHSiH2NHSiH3 silazanes
He 3
He helion
He atomic laser
He+ Rutherford
backscattering (RBS)
4
He -particle (alpha-
particle)
Hg Hg resonance lamp
I I identity reaction
129
I nuclear quadrupole
moment
(spectroscopic)
131
I radioiodination
125
I radioiodination
123
I radioiodination
I excimer lamp
I+ halonium ions
IK IK isotopic scrambling
IO2 IO2 characteristic group in
IXe XeI excimer lamp
I2 I2 dopant
I2 excimer lamp
K K syntectic reaction
KMnO4 KMnO4 equivalent entity
KZn K-Zn syntectic reaction
KZn13 KZn13 syntectic reaction
Kr Kr excimer lamp
Kr resonance lamp
Kr liquid ion laser
Kr2 Kr2 excimer lamp
La La3+ ionic conductivity
Li Li+ order-disorder
transition
LiMn2O4 Li[Mn2]O4 topochemical reaction
Mg Mg solute-volatilization
spectroscopy
Mg2+ selectivity coefficient,
in ion exchange
chromatography
Mg2O4Si Mg2SiO4 reconstructive
transition
MnO2 MnO2 magnetic transition
Mn3O4 Mn3O4 JahnTeller transition
N N imides
N hydrogen bond in
theoretical organic
chemistry
N dipolar compounds
N hydrogen bond
N umpolung
N nitriles
N amidium ions
N alkoxyamines
N spin crossover
NO NO reference procedure in
analysis of trace air
constituents
NO nitroso compounds
NO emission in
NO composition of pure air
in atmospheric
chemistry
N=O isonitroso compounds
NO+ isoelectronic
NO primary pollutant in
NO2 NO2 reference procedure in

constituents
NO2+ electrofuge
NO2 nitro compounds
NO2 -electron
acceptor/donor group
NO2 composition of pure air
in atmospheric
chemistry
NO2 permeation tube
NO2 air pollutant
NO2 electrophile
(electrophilic)
NO3 NO3 mean activity of an
NO3 oxidant in atmospheric
chemistry
NO3Rb RbNO3 thermally-induced
transition
N2 N2 reference procedure in
constituents
N2 cage
=N+=N diazo compounds
N2 molecular laser
N2 photochemical
nitrogen extrusion
N2 isoelectronic
N2 cryogenic sampling
N2 geminate
recombination
N2O N2O local fraction
atomized, , in
flame emission and
absorption
spectrometry
N3 N3 azides
N=N+=N azides
N3 pseudohalogens
N3 quinone diazides
N3Na NaN3 azides
Na Na+ mean activity of an
Na+ interfering substance
chemistry
Na resonance lamp
Na+ ionic conductivity
Nb3Sn Nb3Sn superconducting
transition
Ne Ne heliumneon laser
Ne atomic laser
Ne excimer lamp
Ni 63
Ni electron capture
detector in gas
chromatography
NiS NiS dilational (dilatational)
transition
O O imides
=O hydrazidines
O silathianes
=O characteristic group in
=O imidines
O imidines
O2 ligands
=O hydroximic acids
O dipolar compounds
O hydrogen bond
O tautomerism
O diamidides
=O diamidides
O hydrogen bond in
theoretical organic
chemistry
O silazanes
=O oxo compounds
O umpolung
O ylides
O amidium ions
=O hydrazones
=O imidic acids
O branching chain
reaction
OP PO ligases (synthetases)
O2 O2 biochemical
(biological) oxygen
demand ( )
(=O)2 sulfonediimines
O2 singlet molecular
oxygen (singlet
molecular dioxygen)
O2 spin-statistical factor
(in diffusion-controlled
reactions)
O2 flow rate in flame
emission and
absorption
spectrometry
O2 mean free path,
O22 peroxides
O2 catalase
O2 chemical oxygen
demand ( )
O2 chemical bond
O2 Schenck-sensitization
mechanism
O2 HaberWeiss reaction
O2 HaberWeiss reaction
O2 photosynthesis
O2 configuration
(electronic)
O2S SO2 oxidized species
SO2 extraction (equilibrium)
constant
SO2 emission in
O2S cheletropic reaction
SO2 primary pollutant in
SO2 oxidation state
SO2 permeation tube
SO2 composition of pure air
in atmospheric
chemistry
SO2 sink in atmospheric
chemistry
SO2 air pollutant
O2Si SiO2 polymorphic transition
SiO2 displacive transition
O2Ti TiO2 irreversible transition
O2V VO2 metalinsulator
transition
O2Zr ZrO2 martensitic transition
O3 O3 reference procedure in
constituents
O3 secondary pollution
(emissions)
O3 decay rate in
O3 greenhouse effect in
O3S SO3 oxidized species
SO3 oxidation state
(SO3) membrane sites in an
ion-selective electrode
O3Ti2 Ti2O3 semiconductor-metal
transition
O4 O4 chemical bond
O4S SO42 Brnsted base

SO42 selectivity coefficient,
in ion exchange
chromatography
O4S3 3SO42 mean activity of an
O4Si SiO4 displacive transition
O5P2 P2O5 electrolytic hygrometer
O5V2 V2O5 gel
P P imides
P umpolung
PbS PbS photoconductive
detector
Pt Pt pH
Pt gas sensing electrode
S S polytypic transition
S imides
S tautomerism
S mustards
S silathianes
S hydrogen bond in
theoretical organic
chemistry
S umpolung
S ylides
S poison in catalysis
S triple point
SZn ZnS polytypic transition
S2 S2 polysulfanes
S2Ti TiS2 intercalation reaction
S8 S8 oxidation state
Se Se imides
Se umpolung
Se ylides
Si Si di--silane
rearrangement
Si silanols
Si photoconductive
detector
SiV3 V3Si superconducting
transition
Sn 119
Sn nuclear quadrupole
moment
(spectroscopic)
119
Sn quadrupole splitting in
Mssbauer
spectroscopy
Te Te imides
Te ylides
Ti Ti3+ solid state lasers
U 239
U resonance neutrons
Xe Xe excimer lamp
Xe resonance lamp
Xe2 Xe2 excimer lamp
Zn Zn polytypic transition
Zn syntectic reaction
Zn resonance lamp

IUPAC Gold Book - Sum Formulas

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IUPAC Gold Book - Sum Formulas

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21/11/2017 IUPAC Gold Book - Sum formulas

Ar2 Ar2 excimer lamp

CH2 tropyl radicals

CH3 benzylic intermediates

CH3O+ oxylium ions

CH5B CH5B spectator mechanism

CH5P CH3PH2 phosphines

CO2 cryogenic sampling

CH3CO2 Brnsted base

isotopic molecular ion

C3H8 C3H8 catalytic

C5H5N nucleophilic catalysis

C6H5AsCa CaAsPh arsenides

C6H9Sb (CH2=CH)3Sb stibines

C7H5NO PhOCN cyanates

C7H16 C7H16 catalytic

C8H10S C8H10S leaving group

C9H6O2 C9H6O2 isocoumarins

C12H10O5S2 PhS(=O)2OS(=O)2Ph sulfonic anhydrides

C19H14O5S C19H14O5S sulfonphthaleins

C20H12O5 C20H12O5 xanthene dyes

C40H56O2 C40H56O2 carotenoids

CsCl structural transition

ClH4N NH4Cl structural transition

Cr3+ ruby laser

HN=NH azo compounds

H2SO4 reduced species

(H3O+) onium compounds

H3O3P P(OH)3 oxoacids

H3Te (H3Te+) onium compounds

NO2 NO2 reference procedure in

O4S SO42 Brnsted base

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