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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
interference in flame
spectroscopy
AlCl3 AlCl3 ionization
AlNb3 Nb3Al superconducting
transition
Al2 2Al3+ mean activity of an
electrolyte in solution
Al2MgO4 MgAl2O4 solute-volatilization
interference in flame
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
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
electrolyte in solution
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
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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
atmospheric chemistry
CCl3 carbanion
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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
organic nomenclature
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
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(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
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compounds
C4H7NO (CH3)2C(OH)CN cyanohydrins
C4H7Y C4H7Y chain polymerization
C4H8 C4H8 addition reaction
C4H8 cycloalkanes
C4H8 anti
C4H8 hyperconjugation
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)
C4H9O C4H9O fragmentation
C4H10 C4H10 catalytic
hydrogenolysis
C4H10Mg Et2Mg organometallic
compounds
C4H10N C4H10N pre-equilibrium (prior
equilibrium)
C4H10O C4H10O fragmentation
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
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(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
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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
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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
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NH silazanes
HN Lewis acid
HN= imino acids
HNO =NOH hydroximic acids
HNO2 HON=O oxoacids
HONO smog chamber in
atmospheric chemistry
HNO3 HNO3 smog chamber in
atmospheric chemistry
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
organic nomenclature
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
atmospheric chemistry
OH hydrazides
alcohols
HO.
OH alcohols
OH hydroxamic acids
HO molecular
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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
atmospheric chemistry
OH peroxy acids
HO2 OOH peroxy acids
HO3S SO3H characteristic group in
organic nomenclature
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
organic nomenclature
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
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organic nomenclature
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
interference in flame
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
atmospheric chemistry
NO composition of pure air
in atmospheric
chemistry
N=O isonitroso compounds
NO+ isoelectronic
NO primary pollutant in
atmospheric chemistry
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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
organic nomenclature
=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,
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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
atmospheric chemistry
O2S cheletropic reaction
SO2 primary pollutant in
atmospheric chemistry
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
analysis of trace air
constituents
O3 secondary pollution
(emissions)
O3 decay rate in
atmospheric chemistry
O3 greenhouse effect in
atmospheric chemistry
O3S SO3 oxidized species
SO3 oxidation state
(SO3) membrane sites in an
ion-selective electrode
O3Ti2 Ti2O3 semiconductor-metal
transition
O4 O4 chemical bond
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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
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