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Completely conjugated monocyclic hydrocarbons
Annulenes are monocyclic hydrocarbons that contain the maximum number of non-cumulated or conjugated double bonds ('mancude'), and their derivatives.
Annulene
Chemical compound
or [18]annulene is an organic compound with chemical formula C 18H 18. It belongs to the class of highly conjugated compounds known as annulenes and is
Cyclooctadecanonaene
Chemical compound
Cyclodecapentaene or [10]annulene is an annulene with molecular formula C10H10. This organic compound is a conjugated 10 pi electron cyclic system and
Cyclodecapentaene
Index of chemical compounds with the same name
Methano(10)annulene may refer to: 1,5-Methano(10)annulene 1,6-Methano(10)annulene This set index article lists chemical compounds articles associated with
Methano(10)annulene
Chemical property
as well as most other [n]annulenes CnHn when n is twice an odd number, such as [14]annulene and [18]annulene. [10]annulenes are an exception as they are
Aromaticity
Chemical compound
5-Methano[10]annulene, 1,5-methanoazulene or homoazulene is a hydrocarbon with chemical formula C11H10. Homoaromaticity Cyclodecapentaene 1,6-Methano[10]annulene v
1,5-Methano(10)annulene
Chemical compound
1,6-Methano[10]annulene (also known as 1,6-methanonaphthalene or homonaphthalene) is an aromatic hydrocarbon with chemical formula C11H10. It was the first
1,6-Methano(10)annulene
Compound containing rings with delocalized pi electrons
aromatic compound. Of annulenes larger than benzene, [12]annulene and [14]annulene are weakly aromatic compounds and [18]annulene, Cyclooctadecanonaene
Aromatic_compound
Property of conjugated systems with 4n delocalized electrons
follow Hückel’s 4n+2 π-electron rule. Like its relative [12]annulene, hexadehydro-[12]annulene is also antiaromatic. Its structure has been studied computationally
Antiaromaticity
Chemical reaction
that they had ignored existing literature on Zincke but held on to the annulene structure based on their electrospray ionization (ESI) results which according
Zincke_reaction
Method of determining aromaticity in organic molecules
stability of completely conjugated monocyclic hydrocarbons (known as annulenes) as well as their cations and anions. The best-known example is benzene
Hückel's_rule
Chemical compound
Cyclododecahexaene or [12]annulene (C 12H 12) is a member of the series of annulenes with some interest in organic chemistry with regard to the study of
Cyclododecahexaene
Index of chemical compounds with the same molecular formula
including: Dodecaheptaene, a straight-chain polyene Cyclododecahexaene ([12]annulene) Cyclododecatriyne [6]Radialene(hexaradialene) Ten dimethylnaphthalene
C12H12
Organic chemical compound
the benzene core, making 1,2,4,5,7,8,10,11,13,14,16,17-dodecadehydro[18]annulene. An analog of this molecule, with the hydrogen atoms replaced by phenyl
Carbo-mer
Chemical compound
incorporating elements from the actinide series. It is the most studied bis[8]annulene-metal system, although it has no known practical applications. Uranocene
Uranocene
Chemical compound
antiaromatic hydrocarbon with 4 π electrons. It is the smallest [n]-annulene ([4]-annulene). Its rectangular structure is the result of a pseudo- (or second
Cyclobutadiene
Chemical compound
Cyclotetradecaheptaene, often referred to as [14]annulene, is a hydrocarbon with molecular formula C14H14, which played an important role in the development
Cyclotetradecaheptaene
Chemical compound
Springer. pp. 77–82. ISBN 978-3642707353. Stöckel, K.; Sondheimer, F. "[18]Annulene". Organic Syntheses. 54: 1. doi:10.15227/orgsyn.054.0001; Collected Volumes
Copper(II)_acetate
Conjugated hydrocarbon ring molecules with at least one triple bond
double bonds in addition to at least one triple bond. They are related to annulenes, which only have alternating single and double bonds. The smallest member
Annulyne
Theory of molecular orbitals by Erich Hückel
N-1)} . Energy levels are all distinct. Cyclic system, Hückel topology (annulene/annulenyl): E k = α + 2 β cos 2 k π N ( k = 0 , 1 , … , ⌊ N / 2 ⌋ ) {\displaystyle
Hückel_method
Chemical bond involving six bonding electrons; one sigma plus two pi bonds
Structure and AFM image of dehydrobenzo[12]annulene, where benzene rings are held together by triple bonds
Triple_bond
Rule in organic chemistry
University of Western Ontario in 1972. The lowest triplet state of an annulene is, according to Baird's rule, aromatic when it has 4n π-electrons and
Baird's_rule
CHCl3, historical anaesthetic and common solvent
ISBN 978-0-471-93623-7. Vogel, E.; Klug, W.; Breuer, A. (1988). "1,6-Methano[10]annulene". Organic Syntheses; Collected Volumes, vol. 6, p. 731. Gokel, G. W.; Widera
Chloroform
Index of chemical compounds with the same molecular formula
molecular formula C11H10 may refer to: Methano[10]annulenes 1,5-Methano[10]annulene 1,6-Methano[10]annulene Methylazulenes 1-Methylazulene 2-Methylazulene
C11H10
Chemical compound
trivial name 'corannulene', which is derived from the annulene-within-an-annulene model: core + annulene. However, later theoretical calculations have disputed
Corannulene
Chemical compound
two distinct C–C bond distances. This result indicated that COT is an annulene with fixed alternating single and double C-C bonds. In its normal state
Cyclooctatetraene
Hydrocarbon compound (C3H8)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Propane
Concept in theoretical chemistry
the common global aromaticity observed in single-ring macrocycles like annulenes. The question of whether superaromaticity is a real, significant phenomenon
Superaromaticity
Soluble chemical substance or natural material which can impart color to other materials
phthalocyanine structure. They are structurally related to porphyrins and share the annulene element. By introducing water-soluble substituents—primarily via
Dye
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Ammonia
Chemical compound
1021/om049292t. Vogel, E.; Klug, W.; Breuer, A. (1974). "1,6-Methano[10]annulene". Organic Syntheses. 54: 11. doi:10.15227/orgsyn.054.0011; Collected Volumes
1,4-Benzoquinone
Hydrocarbon compound (CH4) in natural gas
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Methane
Alkane with 5 carbon atoms C5H12
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Pentane
Organic reaction used to convert arenes to cyclohexadienes
Skopje, Macedonia Vogel, E.; Klug, W.; Breuer, A. (1974). "1,6-Methano[10]annulene". Organic Syntheses; Collected Volumes, vol. 6. Edwin M. Kaiser and Robert
Birch_reduction
Chemical compound
S)-1-(3-fluoropropyl)pyrrolidin-3-yl]oxyphenyl]-8,9-dihydro-7H-benzo[7]annulene-2-carboxylic acid CAS Number 2114339-57-8 PubChem CID 130232326 DrugBank
Amcenestrant
Chemical compound (C7H16)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Heptane
Poisonous and flammable gas
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_sulfide
Organic compound (H3C–CH3)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Ethane
Chemical reaction in organic chemistry
Adv. Org. Chem. 1963, 4, 225. K. Stöckel and F. Sondheimer (1974). "[18]Annulene". Organic Syntheses. 54: 1. doi:10.15227/orgsyn.054.0001. I. D. Campbell
Glaser_coupling
Chemical compound
12a-Trimethyl-1,2,4a,5,6,7,8,11,12,12a-decahydro-6,10-methanobenzo[10]annulene Identifiers CAS Number 163594-75-0 3D model (JSmol) Interactive image ChemSpider
Taxadiene
Chemical compound
4-Dioxacyclohexa-2,5-diene Other names 1,4-Dioxin Dioxin p-Dioxin 1,4-Dioxa[6]annulene Identifiers CAS Number 290-67-5 Y 3D model (JSmol) Interactive image ChEBI
1,4-Dioxin
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Styrene
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_peroxide
Hydrocarbon compound (H2C=CH2)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Ethylene
Heterocyclic organic compound,
4-Epoxybuta-1,3-diene 1-Oxacyclopenta-2,4-diene Other names Oxole Oxa[5]annulene 1,4-Epoxy-1,3-butadiene 5-Oxacyclopenta-1,3-diene 5-Oxacyclo-1,3-pentadiene
Furan
Hydrocarbon compound (C6H6)
Cyclohexa-1,3,5-triene; 1,3,5-Cyclohexatriene (theoretical resonance isomers) [6]Annulene (not recommended) Phene (historic) Identifiers CAS Number 71-43-2 Y 3D
Benzene
Hydrocarbon compound containing one or more C=C bonds
quotations related to Alkene. Aromatic hydrocarbon ("Arene") Alpha-olefin Annulene Dendralene Radialene Nitroalkene Wade, L.G. (2006). Organic Chemistry (6th ed
Alkene
Macrocylcic molecule
A cyanostar (pentacyanopentabenzo[25]annulene) is a shape-persistent macrocycle that binds anions. The cyanostar structure is synthesized in a one-pot
Cyanostar
Colorless flammable liquid with an ammonia-like odor
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrazine
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_chloride
Flammable organic fuel (C4H10)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Butane
Organic compounds with the formula (CH3)2C6H4
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Xylene
Form of water
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Heavy_water
Chemical compound
8-bis[(2R,3R)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-2-yl]-5H-benzo[7]annulene-4,6-diyl bis(3,4,5-trihydroxybenzoate) Other names TFDG TF-3 Theaflavin-3
Theaflavin_digallate
Organic compound consisting entirely of hydrogen and carbon
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Hydrocarbon
Physical and chemical properties of pure water
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Properties_of_water
Radioactive form of water
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Tritiated_water
Chemical substance
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_iodide
Special type of aromaticity
Köhler, Felix; Herges, Rainer (2010-04-16). "The [13]Annulene Cation Is a Stable Möbius Annulene Cation". Organic Letters. 12 (8): 1708–1711. doi:10.1021/ol1002384
Möbius_aromaticity
Organic compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Cumene
Chemical reaction
W.; Takada, S.; Masamune, S. (1971). "Concerning the 1,5-didehydro[10]annulene system". J. Chem. Soc. D. 1971 (23): 1516–1517. doi:10.1039/C29710001516
Bergman_cyclization
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Azulene
Aromatic hydrocarbon
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Toluene
Hydrocarbon compound made of a 5-carbon chain with two single and two double bonds
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Pentadiene
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Tetraoxidane
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Pentadienyl
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Americium_trihydride
Computational organic chemist at Imperial College London
Rzepa, H. S. (2005). "A Double-Twist Möbius-Aromatic Conformation of [14]Annulene". Organic Letters. 7 (21): 4637–4639. doi:10.1021/ol0518333. PMID 16209498
Henry_Rzepa
Chemical compound (C6H14)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hexane
Electric current observed in aromatic compounds
cyclooctadecanonaene ([18]annulene) with 6 inner protons at −3 ppm. The situation is reversed in antiaromatic compounds. In the dianion of [18]annulene the inner protons
Aromatic_ring_current
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Naphthalene
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
1-Butene
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Cyclopropyne
Chemical compound
Mitchell and Sondheimer prepared the compound from a benzannulated [10]annulene. A sulfur extrusion method was reported by Kemp, Storie, and Tulloch. Wu
Zethrene
Hydrocarbon composed of multiple aromatic rings
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Polycyclic aromatic hydrocarbon
Polycyclic_aromatic_hydrocarbon
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_fluoride
Swiss-German chemist and professor (1921–2006)
Swiss German chemist. In 1964 he published the concept of Möbius cyclic annulenes, but the first Möbius aromatic was not synthesized until 2003. Edgar Heilbronner
Edgar_Heilbronner
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Lithium_hydride
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
4-Vinyltoluene
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Aluminium_hydride
Type of saturated hydrocarbon compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Alkane
Chemical compound
Siegwarth, Jan; Herges, Rainer (21 December 2009). "Is the [9]Annulene Cation a Möbius Annulene?". Angewandte Chemie International Edition. 48 (52): 9971–9974
Cyclononatetraene
Polyunsaturated organic compound
and double carbon–carbon bonds, with characteristic optical properties. Annulenes are conjugated cyclopolyenes. The following polyenes are used as antifungals
Polyene
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_bromide
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Methylcyclobutane
Hydrocarbon compound (C22H14) made of 5 fused benzene rings
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Pentacene
Saturated alicyclic hydrocarbon
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Cycloalkane
Organic compounds with the empirical formula CH3C6H4CH2CH3
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Ethyltoluene
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Butadiene
Chemical compound (C7H14)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
1-Heptene
Hydrocarbon compound containing one or more C≡C bonds
pub3. ISBN 978-3-527-30673-2. K. Stöckel and F. Sondheimer (1974). "[18]Annulene". Organic Syntheses. 54: 1. doi:10.15227/orgsyn.054.0001. Annabelle L.
Alkyne
Hydrocarbon compound (HC≡CH)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Acetylene
Hydrocarbon compound with the formula C8H18
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Octane
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Diborane
Romanian chemist
[n]annulene valence isomers (CH)n where n is an even number. With two coauthors, Balaban published in 1986 on this topic a 3-volume monograph (Annulenes
Alexandru_Balaban
Chemical compound hydrogen phosphide
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Phosphine
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Semiheavy_water
Unsaturated hydrocarbon compound (H2C=C(CH3)2)
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Isobutylene
Chemical compound (CH3CH=CH2)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Propylene
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Titanium_hydride
ANNULENE
ANNULENE
ANNULENE
ANNULENE
Girl/Female
British, Christian, English, Hebrew, Swedish
Female Version of John; The Lord is Gracious; God is Merciful
Male
Spanish
Spanish form of Latin Ambrosius, AMBROSIO means "immortal."
Girl/Female
African, Anglo, Australian, Chinese, Christian, Hebrew, Indian, Japanese
Goddess of Saraswati
Girl/Female
Tamil
Vidyadevi | விதà¯à®¯à®¾à®¤à¯‡à®µà¯€
Goddess of knowledge
Girl/Female
Assamese, Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Oriya, Sanskrit, Sindhi, Tamil, Telugu, Traditional
Soft; Tenderness; An Ideal Woman; Beautiful
Girl/Female
Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Telugu
Wish; Desire
Boy/Male
Hindu
One of the kauravas
Boy/Male
Tamil
To win others hearts
Boy/Male
Indian
Kind, Friend
Girl/Female
Arabic, Muslim
Flower; Beautiful
ANNULENE
ANNULENE
ANNULENE
ANNULENE
ANNULENE