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TERPHENYL

  • Terphenyl
  • Chemical compound

    are three substitution patterns: ortho-terphenyl, meta-terphenyl, and para-terphenyl. Commercial grade terphenyl is generally a mixture of the three isomers

    Terphenyl

    Terphenyl

    Terphenyl

  • M-Terphenyl
  • Organic ligand

    m-Terphenyls (also known as meta-terphenyls, meta-diphenylbenzenes, or meta-triphenyls) are organic molecules composed of two phenyl groups bonded to

    M-Terphenyl

    M-Terphenyl

    M-Terphenyl

  • Polychlorinated terphenyl
  • Polychlorinated terphenyls (PCTs) are a group of chlorine derivatives of terphenyls. They are chemically related to polychlorinated biphenyls and have

    Polychlorinated terphenyl

    Polychlorinated terphenyl

    Polychlorinated_terphenyl

  • 2,6-Diisopropylphenyl group
  • steric bulk. NacNac ligands can be prepared from 2,6-diisopropylaniline. Terphenyl ligands featuring two diisopropylphenyl substituents, systematically

    2,6-Diisopropylphenyl group

    2,6-Diisopropylphenyl_group

  • Piqua Nuclear Power Facility
  • Nuclear reactor in Ohio, United States

    5-megawatt (thermal) organically cooled and moderated nuclear reactor (terphenyl, a biphenyl like oil). The Piqua facility was built and operated between

    Piqua Nuclear Power Facility

    Piqua Nuclear Power Facility

    Piqua_Nuclear_Power_Facility

  • IUPAC numerical multiplier
  • Value in chemical nomenclature

    1-Trichloro-bis-2,2(4-chlorophenyl)ethane). Examples are biphenyl or terphenyl. "mono-" is from Greek monos = "alone". "un" = 1 and "nona-" = 9 are from

    IUPAC numerical multiplier

    IUPAC_numerical_multiplier

  • Nuclear reactor
  • Device for controlled nuclear reactions

    as a moderator. Organically moderated reactors (OMR) use biphenyl and terphenyl as moderator and coolant. Water-cooled reactor. These constitute the great

    Nuclear reactor

    Nuclear reactor

    Nuclear_reactor

  • Quintuple bond
  • Chemical bond involving ten bonding electrons

    contrast, the chromium dimer with quintuple bonding is stabilized by a bulky terphenyl (2,6-[(2,6-diisopropyl)phenyl]phenyl) ligands. The species is stable up

    Quintuple bond

    Quintuple bond

    Quintuple_bond

  • Para-Quaterphenyl
  • Chemical compound

    It can be considered as next in the series of benzene, biphenyl, para-terphenyl. It is an aromatic hydrocarbon and a chromophore. One possible use is

    Para-Quaterphenyl

    Para-Quaterphenyl

  • Liquid-crystal display
  • Display that uses the light-modulating properties of liquid crystals

    exhibit mutual attraction. Polarizable rod-shaped molecules (biphenyls, terphenyls, etc.) are common. A common form is a pair of aromatic benzene rings,

    Liquid-crystal display

    Liquid-crystal display

    Liquid-crystal_display

  • Hexaphenylbenzene
  • Chemical compound

    Hexaphenylbenzene Names Preferred IUPAC name 23,24,25,26-Tetraphenyl-11,21:22,31-terphenyl Other names Hexaphenylbenzene Identifiers CAS Number 992-04-1 Y 3D model

    Hexaphenylbenzene

    Hexaphenylbenzene

    Hexaphenylbenzene

  • Polyester
  • Category of polymers, in which the monomers are joined together by ester links

    naphthalenes or diphenyls, as well as non-chlorinated aromatics like terphenyls, benzophenones or dibenzylbenzenes. The reaction was also applied successfully

    Polyester

    Polyester

    Polyester

  • Maser
  • Device for producing coherent EM waves in the sub-visible spectrum

    operated at room temperature by using optically pumped, pentacene-doped p-Terphenyl as the amplifier medium. It produced pulses of maser emission lasting

    Maser

    Maser

    Maser

  • Bond order
  • Difference between the number of bonds and anti-bonds in a molecule

    four Cl− ligands by a bond with an order of 1. The compound (terphenyl)–CrCr–(terphenyl) contains two chromium atoms linked to each other by a bond with

    Bond order

    Bond_order

  • Polyporic acid
  • Chemical compound

    Polyporic acid is a para-terphenyl benzoquinone compound first identified by German chemist Stahlschmidt from a mycelial culture of the fungus genus Hapalopilus

    Polyporic acid

    Polyporic acid

    Polyporic_acid

  • Hydnellum caeruleum
  • Species of fungus

    have been isolated from the species including the p-terphenyl compound Aurantiacin and six p-terphenyl derivatives named thelephantins I–N with a known compound

    Hydnellum caeruleum

    Hydnellum caeruleum

    Hydnellum_caeruleum

  • Polychlorinated biphenyl
  • Highly carcinogenic chemical compounds

    ISBN 978-981-13-7462-3. Kimbrough RD, Jensen AA, eds. (2012). Halogenated Biphenyls, Terphenyls, Naphthalenes, Dibenzodioxins and Related Products. Elsevier. p. 24.

    Polychlorinated biphenyl

    Polychlorinated biphenyl

    Polychlorinated_biphenyl

  • Pentacene
  • Hydrocarbon compound (C22H14) made of 5 fused benzene rings

    and lowest unoccupied molecular orbitals. In 2012, pentacene-doped p-terphenyl was shown to be effective as the amplifier medium for a room-temperature

    Pentacene

    Pentacene

    Pentacene

  • Biphenyl
  • Chemical compound

    polychlorinated biphenyls (PCBs). Naphthalene, where the rings are fused Terphenyl, three ringed analog Bithiophene Polypyrrole OMRE, experimental organic

    Biphenyl

    Biphenyl

    Biphenyl

  • Penicillium chermesinum
  • Species of fungus

    chermesinum produces plastatin, luteosporin, xanthomegnin, azaphilones, p-terphenyls and costaclavine. List of Penicillium species Huang, H; Feng, X; Xiao

    Penicillium chermesinum

    Penicillium_chermesinum

  • Short-Baseline Near Detector
  • Experimental particle physics project

    a wavelength shifting coating of either tetraphenyl butadiene or para-terphenyl was applied directly to the optical detector windows as well as a series

    Short-Baseline Near Detector

    Short-Baseline_Near_Detector

  • Cycloparaphenylene
  • of 4,4′-bis(trimethylstannyl)biphenyl and 4,4′ ′-bis(trimethylstannyl)terphenyl, respectively, with Pt(cod)Cl2 (where cod is 1,5-cyclooctadiene) through

    Cycloparaphenylene

    Cycloparaphenylene

    Cycloparaphenylene

  • List of compounds with carbon number 18
  • pentaethylacetophenone 500021-17-0 C18H14 dihydrochrysene 41593-31-1 C18H14 terphenyl 26140-60-3 C18H14ClFN2O3 ethyl loflazepate 29177-84-2 C18H14Cl4N2O miconazole

    List of compounds with carbon number 18

    List_of_compounds_with_carbon_number_18

  • Congener (chemistry)
  • Related substances

    polychlorinated dibenzodioxins, polychlorinated dibenzofurans, polychlorinated terphenyls, polychlorinated naphthalene, polychloro phenoxy phenol, and polybrominated

    Congener (chemistry)

    Congener (chemistry)

    Congener_(chemistry)

  • Organothallium chemistry
  • Organometallic compounds of thallium

    Reactivity of Dimeric Ar'TlTlAr' and Trimeric (Ar' 'Tl)3 (Ar', Ar' ' = Bulky Terphenyl Group) Thallium(I) Derivatives: Tl(I)−Tl(I) Bonding in Species Ligated

    Organothallium chemistry

    Organothallium_chemistry

  • Reichardt's dye
  • Chemical compound

    Preferred IUPAC name 25-(2,4,6-Triphenylpyridin-1-ium-1-yl)[11,21:23,31-terphenyl]-22-olate Identifiers CAS Number 10081-39-7 3D model (JSmol) Interactive

    Reichardt's dye

    Reichardt's dye

    Reichardt's_dye

  • Single-photon source
  • Technique in quantum optics

    the 1980s. Subsequently, single pentacene molecules were detected in p-terphenyl crystals. The single molecules have begun to be utilised as single-photon

    Single-photon source

    Single-photon_source

  • Bisphenol Z
  • Chemical compound

    Z Names Preferred IUPAC name 23,24,25,26-Tetrahydro-22H-[11,21:21,31-terphenyl]-14,34-diol Other names Bis(4-hydroxyphenyl)cyclohexane Identifiers CAS

    Bisphenol Z

    Bisphenol Z

    Bisphenol_Z

  • Poly(2,6-diphenylphenylene oxide)
  • Chemical compound

    poly(oxy -2,6-diphenyl-1,4-phenylene) Other names poly(oxy[1,1′:3′,1′′-terphenyl]-2′,5′-diyl), poly(2,6-diphenylphenol), poly(2,6-diphenyl-p-phenylene

    Poly(2,6-diphenylphenylene oxide)

    Poly(2,6-diphenylphenylene oxide)

    Poly(2,6-diphenylphenylene_oxide)

  • UiO MOFs
  • UiO series of metal-organic frameworks

    organic linkers are terepthalic acid, biphenyl-4,4′-dicarboxylic acid, terphenyl-4,4''-dicarboxylic acid, and quaterphenyl-4,4'-dicarboxylic acid for UiO-66

    UiO MOFs

    UiO MOFs

    UiO_MOFs

  • Aluminylene
  • The first free aluminylene came from Tuononen and Power, who used bulky terphenyl ligands to stabilize the reduction of the aluminium(III) diiodide.  The

    Aluminylene

    Aluminylene

    Aluminylene

  • Mallory reaction
  • Organic chemical reaction

    factors favor the formation of 1 over 2 in a ratio of 98.5:1.5. ortho-Terphenyl substrates cyclize to the corresponding triphenylenes in the presence

    Mallory reaction

    Mallory reaction

    Mallory_reaction

  • Nuclear power in Canada
  • Whitshell Laboratories in Pinawa, Manitoba. 2,739 litres of coolant oil (terphenyl isomer) leaked, most of it into the Winnipeg River, and three fuel elements

    Nuclear power in Canada

    Nuclear_power_in_Canada

  • Immediately dangerous to life or health
  • Exposure to dangerous levels of airborne contaminants

    5 mg/m3 - 107493 92-06-8 - m-Terphenyl 500 mg/m3 - 26140603 84-15-1 1525 o-Terphenyl 500 mg/m3 - 26140603 92-94-4 - p-Terphenyl 500 mg/m3 - 26140603 76-11-9

    Immediately dangerous to life or health

    Immediately dangerous to life or health

    Immediately_dangerous_to_life_or_health

  • Wavelength shifter
  • one or more benzene-ring(s) (e.g. de:1,4-Bis(2-methylstyryl)benzol or p-Terphenyl) since the σ s {\displaystyle \sigma _{s}} and σ p {\displaystyle \sigma

    Wavelength shifter

    Wavelength_shifter

  • Diradicaloid
  • Chemical radical

    agents (Figure 8). The bulky terphenyl and hypersilyl groups provide kinetic stabilization, preventing dimerization. The terphenyl-substituted diradicaloid

    Diradicaloid

    Diradicaloid

  • PCT
  • Topics referred to by the same term

    Personal Communication Telephone, a mobile telephone service Polychlorinated terphenyl, an industrial chemical Polycyclohexylenedimethylene terephthalate, a

    PCT

    PCT

  • Organic nuclear reactor
  • Nuclear reactor cooled or moderated by an organic liquid

    commercialized. Organic reactors use an organic hydrocarbon fluid, such as terphenyl, to cool the reactor core or to moderate neutrons. Several designs use

    Organic nuclear reactor

    Organic nuclear reactor

    Organic_nuclear_reactor

  • Cardo polymer
  • Subgroup of polymers

    separation properties of novel polyimides containing cardo and tert-butyl-m-terphenyl moieties". Express Polymer Letters. 12 (5): 479–489. doi:10.3144/expresspolymlett

    Cardo polymer

    Cardo polymer

    Cardo_polymer

  • Dispersion stabilized molecules
  • reactive moieties within a molecule. In this case bulky ligands like terphenyls, bulky alkoxides, aryl-substituted NHCs, etc. serve as a protective wrapper

    Dispersion stabilized molecules

    Dispersion_stabilized_molecules

  • Endocrine disruptor
  • Chemicals that can interfere with endocrine or hormonal systems

    21 August 2010. Retrieved 14 March 2009. Polychlorinated biphenyls and terphenyls, Environmental Health Criteria monograph No. 002, Geneva: World Health

    Endocrine disruptor

    Endocrine disruptor

    Endocrine_disruptor

  • Borirene
  • Chemical compound

    Due to their inherent reactivity, sterically demanding groups such as m-terphenyl or mesityl substituents are commonly employed to enhance kinetic stability

    Borirene

    Borirene

    Borirene

  • Atromentin
  • Chemical compound

    atromentin Names Preferred IUPAC name 14,23,26,34-Tetrahydroxy[11,21:24,31-terphenyl]-22,25-dione Other names 2,5-Dihydroxy-3,6-bis(4-hydroxyphenyl)-1,4-benzoquinone

    Atromentin

    Atromentin

    Atromentin

  • Organic Moderated Reactor Experiment
  • Decommissioned nuclear reactor experiment in Idaho

    thermal neutron flux, with flexibility to test other polyphenyls such as terphenyl. The design criteria stated included: Maximum fuel surface temperature

    Organic Moderated Reactor Experiment

    Organic Moderated Reactor Experiment

    Organic_Moderated_Reactor_Experiment

  • Coordination number
  • Number of atoms, molecules or ions bonded to a molecule or crystal

    instance of a metal adopting a coordination number of 1 occurs in the terphenyl-based arylthallium(I) complex 2,6-Tipp2C6H3Tl, where Tipp is the 2,4

    Coordination number

    Coordination_number

  • Peptidomimetic
  • Class of compounds designed to mimic features of peptides

    Justin T.; Hamilton, Andrew D. (2001-06-01). "Toward Proteomimetics: Terphenyl Derivatives as Structural and Functional Mimics of Extended Regions of

    Peptidomimetic

    Peptidomimetic

    Peptidomimetic

  • Flavogallonic acid
  • Chemical compound

    Names Preferred IUPAC name 14,15,25,34,35,36-Hexahydroxy[11,21:24,31-terphenyl]-12,22,32-tricarboxylic acid Identifiers 3D model (JSmol) Interactive

    Flavogallonic acid

    Flavogallonic acid

    Flavogallonic_acid

  • Coolant
  • Substance used to reduce or regulate the temperature of a system

    and stability to 400 °C. Polychlorinated biphenyls and polychlorinated terphenyls were used in heat transfer applications, favored due to their low flammability

    Coolant

    Coolant

  • Phellodon
  • Genus of tooth fungi in the family Bankeraceae

    nigernin A and B; a nitrogenous terphenyl derivative, phellodonin; 2',3'-diacetoxy-3,4,5',6',4''-pentahydroxy-p-terphenyl; grifolin; and 4-O-methylgrifolic

    Phellodon

    Phellodon

    Phellodon

  • Phellodon niger
  • Species of fungus

    diterpenoids, nigernin A and B; a terphenyl derivative called phellodonin (2',3'-diacetoxy-3,4,5',6',4''-pentahydroxy-p-terphenyl); grifolin; and 4-O-methylgrifolic

    Phellodon niger

    Phellodon niger

    Phellodon_niger

  • Scintillator
  • Material which glows when excited by ionizing radiation

    scintillators in an organic solvent. The typical solutes are fluors such as p-terphenyl (C 18H 14), PBD (C 20H 14N 2O), butyl PBD (C 24H 22N 2O), PPO (C 15H 11NO)

    Scintillator

    Scintillator

    Scintillator

  • Hydnellum
  • Genus of fungi in the family Bankeraceae

    and learning. Hydnellum caeruleum and H. concrescens have several para-terphenyl derivatives named thelephantins (specifically, variants thelephantins

    Hydnellum

    Hydnellum

    Hydnellum

  • Plumbylene
  • Divalent organolead(II) analogues of carbenes

    PMID 19630390. Pu, Lihung; Twamley, Brendan; Power, Philip P. (2000). "Terphenyl Ligand Stabilized Lead(II) Derivatives of Simple Organic Groups: Characterization

    Plumbylene

    Plumbylene

    Plumbylene

  • Thelephantins
  • Chemical compound

    Thelephora aurantiotincta. Chemically, they are classified as polyphenols and terphenyl derivatives. Three variants (thelephantin A, B, C) have been elucidated

    Thelephantins

    Thelephantins

    Thelephantins

  • Anidulafungin
  • Antifungal medication

    others Other names LY303366, (4R,5S)-4,5-Dihydroxy-N2-[[4''-(pentyloxy)-p-terphenyl-4-yl]carbonyl]-L-ornithyl-L-threonyl-trans-4-hydroxy-L-prolyl-(S)-4-h

    Anidulafungin

    Anidulafungin

    Anidulafungin

  • Center for Pharmaceutical Research and Innovation
  • Prendergast, MA; Thorson, JS (5 June 2015). "Terfestatins B and C, new p-terphenyl glycosides produced by Streptomyces sp. RM-5-8". Organic Letters. 17 (11):

    Center for Pharmaceutical Research and Innovation

    Center_for_Pharmaceutical_Research_and_Innovation

  • List of UN numbers 3101 to 3200
  • Numbers, classes, and proper shipping names allocated to dangerous goods

    biphenyls, liquid or Polyhalogenated terphenyls, liquid UN 3152 9 Polyhalogenated biphenyls, solid or Polyhalogenated terphenyls, solid UN 3153 2.1 Perfluoro(methyl

    List of UN numbers 3101 to 3200

    List_of_UN_numbers_3101_to_3200

  • Supramolecular chemistry
  • Branch of chemistry

    spacers and connecting groups include polyether chains, biphenyls and terphenyls, and simple alkyl chains. The chemistry for creating and connecting these

    Supramolecular chemistry

    Supramolecular chemistry

    Supramolecular_chemistry

  • Group 13/15 multiple bonds
  • Characterization of the Monomeric Imides Ar'MNAr' ' (M = Ga or In; Ar' or Ar' ' = Terphenyl Ligands) with Two-Coordinate Gallium and Indium". Journal of the American

    Group 13/15 multiple bonds

    Group_13/15_multiple_bonds

  • List of MeSH codes (D02)
  • 455.426.559.389.750 – sulfanilic acids MeSH D02.455.426.559.389.805 – terphenyl compounds MeSH D02.455.426.559.389.805.700 – polychloroterphenyl compounds

    List of MeSH codes (D02)

    List_of_MeSH_codes_(D02)

  • Terpyridine
  • Chemical compound

    Nicotelline - isomer of terpyridine Chelating ligand Pincer ligand Terthiophene Terphenyl Lide, D. R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton

    Terpyridine

    Terpyridine

    Terpyridine

  • Kumada coupling
  • Cross coupling reaction in organic chemistry

    Reagents with Bromochlorobenzenes a Novel Synthetic Method of Unsymmetrical Terphenyl". Synthetic Communications. 21 (3): 481–487. doi:10.1080/00397919108016772

    Kumada coupling

    Kumada_coupling

  • Bismuthinidene
  • Class of organobismuth compounds

    modified version of Dostál's bismuthinidene with ketimine arms and m-terphenyl substituents on the ketimine nitrogen atoms disfavors dimerization, instead

    Bismuthinidene

    Bismuthinidene

    Bismuthinidene

  • Halobenzene
  • Index of chemical compounds with the same name

    Luis A.; Miguez, Jose M. Antelo; Hii, K. K. (M.) (2009). "Synthesis of Terphenyls". Organic Preparations and Procedures International. 41 (5): 331–358.

    Halobenzene

    Halobenzene

  • Terthiophene
  • Chemical compound

    building block for the organic semi-conductor polythiophene. Biphenyl Terphenyl Terpyridine "2,2':5',2"-Terthiophene". pubchem.ncbi.nlm.nih.gov. Smeets

    Terthiophene

    Terthiophene

    Terthiophene

  • Rotterdam Convention
  • United Nations treaty

    Polybrominated biphenyls (PBBs) Polychlorinated biphenyls (PCBs) Polychlorinated terphenyls (PCTs) Terbufos Tetraethyl lead Tetramethyl lead Thiram (certain formulations)

    Rotterdam Convention

    Rotterdam Convention

    Rotterdam_Convention

  • Boletopsis grisea
  • Species of fungus

    and lime used to increase timber production. Research has identified p-terphenyl compounds that impart a free radical scavenging activity in laboratory

    Boletopsis grisea

    Boletopsis grisea

    Boletopsis_grisea

  • Hydnellum aurantiacum
  • Species of fungus

    characteristic orange color of H. aurantiacum has been identified as the p-terphenyl compound named aurantiacin. This dark red pigment, a derivative of the

    Hydnellum aurantiacum

    Hydnellum aurantiacum

    Hydnellum_aurantiacum

  • Penicillium raistrickii
  • Species of fungus

    Gloer, K. B.; Gloer, J. B.; Wicklow, D. T.; Dowd, P. F. (1998). "New p-terphenyl and polyketide metabolites from the sclerotia of Penicillium raistrickii"

    Penicillium raistrickii

    Penicillium_raistrickii

  • Dimetallene
  • Chemical compounds with metal to metal double bonds

    elements can be prepared by taking advantage of steric effects from large m-terphenyl ligands. With the production of a substituted dialumene in 2017, metallenes

    Dimetallene

    Dimetallene

  • Single-molecule experiment
  • Single pentacene molecules detected by fluorescence excitation in a p-terphenyl crystal, Phys. Rev. Lett. 65, 2716–2719 (1990) Kneipp, Katrin; Wang, Yang;

    Single-molecule experiment

    Single-molecule experiment

    Single-molecule_experiment

  • Aspergillus candidus
  • Species of fungus

    (GMS) stain. Aspergillus candidus secretes cytotoxic metabolites like terphenyl compounds and terprenins, as well as citrinin and immunotoxic (1→3)-β-D-glucans

    Aspergillus candidus

    Aspergillus candidus

    Aspergillus_candidus

  • Bruno Rossi
  • Italian-American experimental physicist (1905–1993)

    Because solid scintillating material was unavailable, they decided to use terphenyl dissolved in benzine, which is an efficient liquid scintillator. With

    Bruno Rossi

    Bruno Rossi

    Bruno_Rossi

  • Thelephoric acid
  • Chemical compound

    Shiro M, Koyama K (2014). "Potential anti-angiogenesis effects of p-terphenyl compounds from Polyozellus multiplex". Journal of Natural Products. 77

    Thelephoric acid

    Thelephoric acid

    Thelephoric_acid

  • Polyozellus multiplex
  • Species of fungus

    Lee, K. B.; Yoo, I. D.; Song, K. S. (July 2000). "Kynapcin-12, a new p-terphenyl derivative from Polyozellus multiplex, inhibits prolyl endopeptidase"

    Polyozellus multiplex

    Polyozellus multiplex

    Polyozellus_multiplex

  • Biphenylene
  • Chemical compound

    two-step interpolymer dehydrofluorination of an adsorbed halogenated terphenyl molecule polymerization yielded ultraflat four- and eight-membered rings

    Biphenylene

    Biphenylene

    Biphenylene

  • Stibinidene
  • Class of organoantimony compounds

    6-bis-[bis(trimethylsilyl)methyl]-4-[tris(trimethylsilyl)methyl]phenyl, and various m-terphenyl ligands, exist as dimers with the formula RSb=SbR. 2 RSb → RSb=SbR RSb=SbR

    Stibinidene

    Stibinidene

    Stibinidene

  • Organoberyllium chemistry
  • Organoberyllium Complex in Main Group Chemistry

    reported. The phenyl derivative is represented by trimeric Be3Ph6. A terphenyl derivative is known. With bulky aryl ligands three-coordination is observed

    Organoberyllium chemistry

    Organoberyllium chemistry

    Organoberyllium_chemistry

  • N-Heterocyclic carbene boryl anion
  • Isoelectronic structure

    donated by the ligand. These molecules are synthesized by first have m-terphenyls as the ligands on the metal, and then an isolobal exchange occurs, placing

    N-Heterocyclic carbene boryl anion

    N-Heterocyclic carbene boryl anion

    N-Heterocyclic_carbene_boryl_anion

  • Mesquitol
  • Chemical compound

    8-pentahydroxyflavans: atropisomerism and conformation of biphenyl and m-terphenyl analogues from Prosopis glandulosa ('mesquite')". Journal of the Chemical

    Mesquitol

    Mesquitol

    Mesquitol

  • Nocardiopsis gilva
  • Species of bacterium

    Luo, Yinggang (27 March 2013). "Isolation and Characterization of New p-Terphenyls with Antifungal, Antibacterial, and Antioxidant Activities from Halophilic

    Nocardiopsis gilva

    Nocardiopsis_gilva

  • 2012 in science
  • develop the world's first room-temperature maser, using a crystal of p-Terphenyl to modify a commercial medical laser to produce coherent microwave emissions

    2012 in science

    2012_in_science

  • Timeline of nuclear power
  • organic nuclear reactor, cooled and moderated by hydrocarbons, in this case terphenyls, achieves criticality at the Idaho National Laboratory. 1958 On September

    Timeline of nuclear power

    Timeline_of_nuclear_power

  • Phosphaalkyne
  • Class of chemical compounds

    Waugh, Mark (2007-10-15). "Synthesis and structural characterization of a terphenyl substituted phosphaalkyne, PC{C6H3(C6H2Me3-2,4,6)2-2,6}". Journal of Organometallic

    Phosphaalkyne

    Phosphaalkyne

    Phosphaalkyne

  • Organotechnetium chemistry
  • "Structural and Redox Variations in Technetium Complexes Supported by m -Terphenyl Isocyanides". Organometallics. 39 (12): 2287–2294. doi:10.1021/acs.organomet

    Organotechnetium chemistry

    Organotechnetium_chemistry

  • Hapalopilus rutilans
  • Species of fungus

    neurotoxic if ingested. The toxin was identified as polyporic acid, a terphenyl compound first identified from a mycelial culture of the fungus in 1877

    Hapalopilus rutilans

    Hapalopilus rutilans

    Hapalopilus_rutilans

  • Ustalic acid
  • Chemical compound

    T; Isobe, M; Kawagishi, H (2006). "Syntheses of naturally occurring terphenyls and related compounds". Bioscience, Biotechnology, and Biochemistry. 70

    Ustalic acid

    Ustalic acid

    Ustalic_acid

  • WR-1
  • Retired Canadian nuclear research reactor

    OS-84, is a mixture of terphenyls treated catalytically with hydrogen to produce 40 percent saturated hydrocarbons. The terphenyls are petrochemical derivatives

    WR-1

    WR-1

  • Nonahydroxytriphenic acid
  • Chemical compound

    Preferred IUPAC name 14,15,16,23,24,25,34,35,36-Nonahydroxy[11,21:23,31-terphenyl]-12,22,32-tricarboxylic acid Other names Nonahydroxytriphenoyl Identifiers

    Nonahydroxytriphenic acid

    Nonahydroxytriphenic acid

    Nonahydroxytriphenic_acid

  • Quelet reaction
  • Chemical reaction

    halogenated aromatic compounds, aromatic compounds with nitro groups, and terphenyls cannot be used as reactants for Quelet reactions. Even for compounds that

    Quelet reaction

    Quelet reaction

    Quelet_reaction

  • Kynapcin
  • Class of chemical compounds

    Lee HJ, Rhee IK, Lee KB, Yoo ID, Song KS (2000). "Kynapcin-12, a new p-terphenyl derivative from Polyozellus multiplex, inhibits prolyl endopeptidase"

    Kynapcin

    Kynapcin

    Kynapcin

  • Organobismuth radical
  • Chemical radical

    pyridine-dipyrolide ligands (discovered by Turner in 2019) and Bi biradicals with N-terphenyl ligands (discovered by Schulz and coworkers in 2018). In 2015, the first

    Organobismuth radical

    Organobismuth radical

    Organobismuth_radical

  • Digermyne
  • Class of chemical compounds

    2850(6) Å between two Ge atoms. It has a good conjugation between two terphenyl rings and C1-Ge1-Ge2-C2 plain because of the nearly zero torsion angle

    Digermyne

    Digermyne

    Digermyne

  • Pseudoparmelia
  • Genus of lichens

    related genera. A unique chemical feature of the genus is the presence of terphenyl derivatives called butlerins, compounds that are uncommon in lichen-forming

    Pseudoparmelia

    Pseudoparmelia

    Pseudoparmelia

  • Trifucol
  • Chemical compound

    Trifucol Names Preferred IUPAC name [11,21:23,31-Terphenyl]-12,14,16,22,24,26,32,34,36-nonol Identifiers CAS Number 62218-04-6 Y 3D model (JSmol) Interactive

    Trifucol

    Trifucol

    Trifucol

  • Anthracophyllum archeri
  • Species of fungus

    Spatafora, Valeria Calì Carmela; Corrado, Tringali (2003). "Polyhydroxy-P-Terphenyls and Related P-Terphenylquinones From Fungi: Overview and Biological Properties"

    Anthracophyllum archeri

    Anthracophyllum archeri

    Anthracophyllum_archeri

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Online names & meanings

  • Prasen
  • Boy/Male

    Arabic, British, Indian, Marathi

    Prasen

    Siva

  • Flitton
  • Surname or Lastname

    English

    Flitton

    English : habitational name from a place in Bedfordshire called Flitton. The meaning of the place name, recorded in Domesday Book (1086) as Flictham, is unexplained.

  • Gladys
  • Girl/Female

    Latin American French Welsh

    Gladys

    Sword.

  • Rawahah
  • Boy/Male

    Muslim/Islamic

    Rawahah

    Departure Fragrance, ease

  • Rathtyen
  • Girl/Female

    Welsh

    Rathtyen

    Legendary daughter of Clememyl.

  • INNOKENTIY
  • Male

    Russian

    INNOKENTIY

    (Инокентий) Russian form of Latin Innocentius, INNOKENTIY means "harmless, innocent."

  • Vardan
  • Boy/Male

    French

    Vardan

    From the green hill.

  • Ashima | அஷிமா
  • Girl/Female

    Tamil

    Ashima | அஷிமா

    Limitless, Protector

  • Banan
  • Girl/Female

    Muslim

    Banan

    Delicate.

  • Rupaka
  • Boy/Male

    Indian, Sanskrit, Telugu

    Rupaka

    Sign

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