Vicipéid

Liosta na ngás

Is liosta é seo de gháis ar dálaí caighdeánacha, rud a chiallaíonn substaintí a nó a fhiuchann nó a néalaíonn ag 25 nó faoi bhun 25 °C agus ag 1 brú atmaisféarach agus go bhfuil siad réasúnta cobhsaí

Ocsaigin leachtach fiuchta

Liosta cuir in eagar

Déantar an liosta seo a shórtáil de réir fiuchphointe na ngás in ord ardaitheach, ach is féidir é a shórtáil ar luachanna éagsúla. tagraíonn "fo" agus "tríarach" don néalphointe agus don tríphointe, a thugtar i gcás substainte a néalaíonn ag 1 brú atmaisféarach; agran íon"dian" do dhianscaoileadh . ciallaíonn "~" cothrom le.

Ainm Foirmle Fiuchphointe (°C) Leáphointe (°C) Meáchan móilíneach Uimhir CAS
Héiliam-3 3He −269.96 N/A 3 14762-55-1
Héiliam-4 4He −268.928 N/A 4 7440-59-7
Hidrigin H2 −252.879 −259.16 2 1333-74-0
Deoitéiriam[1] D2 −249.49 −254.43 4 7782-39-0
Tritium[2] T2 −248.12 −254.54 6 10028-17-8
Neon Ne −246.046 −248.59 20 7440-01-9
Nítrigin N2 −195.795 −210.0 28 7727-37-9
Aonocsaíd charbóin CO −191.5 −205.02 28 630-08-0
Fluairín F2 −188.11 −219.67 38 7782-41-4
Argón Ar −185.848 −189.34 40 7440-37-1
Ocsaigin O2 −182.962 −218.79 32 7782-44-7
Meatán CH4 −161.5 −182.50 16 74-82-8
Crioptón Kr −153.415 −157.37 84 7439-90-9
Ocsaíd nítreach NO −151.74 −163.6 30 10102-43-9
Défhluairíd ocsaigine F2O −144.3 −223.8 54 7783-41-7
Teitreafhluairíd mheatáin CF4 −127.8 −183.6 88 75-73-0
Trífhluairíd nítrigine NF3 −128.74 −206.79 71 7783-54-2
Siolán SiH4 −111.9 −185 32 7803-62-5
Défhluairíd dénítrigine N2F2 −111.45 −172 66 13776-62-0
Ózón O3 −111.35 −193 48 10028-15-6
Xeanón Xe −108.099 −111.75 131 7440-63-3
cis-Difluorodiazine N2F2 −105.75 −195 66 13812-43-6
Eitiléin CH2=CH2 −103.7 −169.2 28 74-85-1
Phosphorus(III) fluoride PF3 −101.8 −151.5 88 7783-55-3
Chlorine fluoride ClF −101.1 −155.6 54.5 7790-89-8
Boron trifluoride BF3 −99.9 −126.8 68 7637-07-2
Fluorosilane SiH3F −98.6 50 13537-33-2
Trifluorosilane SiHF3 −95 −131 86 13465-71-9
Trifluoromethyl hypofluorite[3] CF3OF −95 −215 104 373-91-1
Débhórán B2H6 −92.49 −164.85 28 19287-45-7
3,3-Difluorodiazirine[4] CF2N2 −91.3 78 693-85-6
Aicéitiléin CH≡CH −84.7 −81.5 26 74-86-2
Ethane CH3CH3 −88.5 −182.8 30 74-84-0
Germane GeH4 −88.1 −165 77 7782-65-2
Ocsaíd nítriúil N2O −88.48 −90.8 44 10024-97-2
Foisfín PH3 −87.75 −133.8 34 7803-51-2
Trifluoramine oxide NOF3 −87.5 −161 87 13847-65-9
Tetrafluorosilane SiF4 −86 −90.2 104 7783-61-1
Trifluoronitrosomethane CF3NO −85 −196.6 99 334-99-6
Azidotrifluoromethane CF3N3 −85 −152 111 3802-95-7
Clóiríd hidrigine HCl −85 −114.17 36.5 7647-01-0
1,1-Difluoroethene CF2=CH2 −85.5 −144 64 75-38-7
Phosphorus(V) fluoride PF5 −84.6 −93.8 126 7647-19-0
Carbonyl fluoride COF2 −84.5 −111.2 66 353-50-4
Trífhluaraimeatán CHF3 −82.1 −155.2 70 75-46-7
Clóirtrífhluaraimeatán CClF3 −81.5 −181 104.5 75-72-9
Bis(difluoroboryl)methane[3] BF2CF2BF2 −81.4 ? 148 55124-14-6
Trifluoroisocyanomethane CF3NC −80 95 105879-13-8
Difluoromethylborane CH3BF2 −78.5 64 373-64-8
Dé-ocsaíd charbóin CO2 −78.464 sub −56.561 triple 44 124-38-9
Fluoromethane CH3F −78.4 −137.8 34 593-53-3
Hexafluoroethane CF3CF3 −78.1 −100.015 138 76-16-4
Pentafluoromethanamine CF3NF2 −78 −130 121 335-01-3
Difluorosilane SiH2F2 −77.8 −122 68 13824-36-7
Tetrafluoroethene CF2=CF2 −76 −131.14 100 116-14-3
Fluoroacetylene FCCH −74 −196 44 2713-09-9
Tetrafluorohydrazine N2F4 −74 −164.5 104 10036-47-2
Nitryl fluoride NO2F −72.4 −166 65 10022-50-1
Fluoroethene CH2FCH3 −72 −160.5 48 75-02-5
Chlorotrifluorosilane SiClF3 −70 −138 120.5 14049-36-6
Trifluoroacetonitrile CF3CN −68.8 95 353-85-5
Nitrogen chloride difluoride NClF2 −67 −195 87.5 13637-87-1
Bróimíd hidrigine HBr −66.38 −86.80 81 10035-10-6
Difluorophosphine[5] PHF2 −65 −124 70 14984-74-8
Borane carbonyl BH3CO −64 −137 42 13205-44-2
Fluoroperoxytrifluoromethane[6] CF3OOF −64 120
Bis(fluoroxy)difluoromethane[7] CF2(OF)2 −64 120 16282-67-0
Sulfur hexafluoride SF6 −63.8 −49.596 triple 146 2551-62-4
TetrafluorooxiraneTeimpléad:Citation needed C2F4O −63.5 116 694-17-7
Airsín AsH3 −62.5 −166 78 7784-42-1
Thiocarbonyl fluoride[8] CSF2 −62.1 −163.5 82 420-32-6
Radón Rn −61.7 −71 222 10043-92-2
Difluorocyanamide[3][9] NF2CN −61 −196 78 7127-18-6
Nitrosyl fluoride ONF −59.9 −132.5 49 7789-25-5
Suilfíd hidrigine H2S −59.55 −85.5 34 7783-06-4
Trifluoroacetyl fluoride[10] CF3COF −59 −159.5 116 354-34-7
Hexafluorodimethyl ether[11] CF3OCF3 −59 154 333-36-8
Bromotrifluoromethane CBrF3 −57.75 −167.78 149 75-63-8
Difluoroaminooxyperfluoromethane[3][12] CF3ONF2 −57.63 137 4217-93-0
Siolán meitile CH3SiH3 −57.5 −156.5 46 992-94-9
Difluorine dioxide F2O2 −57 dec −163.5 70 7783-44-0
Sulfuryl fluoride SO2F2 −55.4 −135.8 102 2699-79-8
Dichlorofluorosilane SiHCl2F −54.3 119 19382-74-2
trans-1,2-Difluoroethene CHF=CHF −53.1 64 1630-78-0
Trifluoroethene CF2=CHF −53 82 359-11-5
Arsenic(V) fluoride AsF5 −52.8 −79.8 170 7784-36-3
Phosphorothioic trifluoride PSF3 −52.25 −148.8 120 2404-52-6
Difluoromethane CH2F2 −52 −136 52 75-10-5
Difluoroamino carbonyl fluoride[13][14] F2NCOF −52 −152.2 99 2368-32-3
Stannane SnH4 −51.8 −146 123 2406-52-2
Tetrafluoropropyne[15] CF3C≡CF −50.39 112 20174-11-2
Carbon oxysulfide OCS −50.2 −138.8 60 463-58-1
Pentafluoroethyl hypofluorite[16] C2F5OF −50 154
Chlorodifluorosilane[17] SiHClF2 −50~ 102.5 80003-43-6
Digallane Ga2H6 −50~ 145.494 12140-58-8
Eitéanón CH2=C=O −49.7 −151 42 463-51-4
Sulfur fluoride oxide SOF4 −48.5 −99.6 124 13709-54-1
3,3,3-Trifluoro-1-propyne CF3CCH −48.3 94 661-54-1
Pentafluoroethane CF3CHF2 −48.1 −100.6 120 354-33-6
Própán C3H6 −47.6 −185.2 42 115-07-1
Phosphorus(III) chloride difluoride PClF2 −47.3 −164.8 104.5 14335-40-1
Carbonyl chloride fluoride COClF −47.2 −148 82.5 353-49-1
1,1,1-Trifluoroethane CF3CH3 −47 −111.8 84 420-46-2
Trifluoromethylhypochlorite[3] CF3OCl −47 −164 120.5 22082-78-6
Perchloryl fluoride ClO3F −46.75 −147 102.5 7616-94-6
Selenium hexafluoride SeF6 −46.6 sub −34.6 triple 193 7783-79-1
Cyanogen fluoride FCN −46 −82 45 1495-50-7
Fluorine nitrate FNO3 −46 −175 81 7789-26-6
Pentafluoronitrosoethane[18] C2F5NO −45.7 137 354-72-3
Difluoromethylene dihypofluorite[19] CF2(OF)2 −45.8 −142 120 16282-67-0
cis-1,2-Difluoroethene CHF=CHF −45 64 1630-77-9
1,1-Difluoropropene[3] CH3CH=CF2 −44 78 430-63-7
DimethylfluoroboraneTeimpléad:Citation needed (CH3)2BF −44 60 353-46-8
Fluoro(trifluoromethyl)silane[20] CF3SiH2F −44 118
Thionyl fluoride SOF2 −43.8 −110.5 86 7783-42-8
Phosphorus(V) chloride tetrafluoride PClF4 −43.4 −132 142.5 13498-11-8
Methyldiborane CH3B2H5 −43 42 23777-55-1
Difluoro(trifluoromethyl)phosphine[21] CF3PF2 −43 138 1112-04-5
N,N,1,1-Tetrafluoromethylamine[22] CHF2NF2 −43 103 24708-53-0
Propane C3H8 −42.25 −187.7 44 74-98-6
Trifluoro(trifluoromethyl)silane[23] CF3SiF3 −42 154 335-06-8
Bromotrifluorosilane BrSiF3 −41.7 −70.5 169 14049-39-9
Hydrogen selenide H2Se −41.25 −65.73 81 7783-07-5
Chlorodifluoromethane CHClF2 −40.7 −175.42 86.5 75-45-6
Sulfur tetrafluoride SF4 −40.45 −125 108 7783-60-0
Hexafluorodiazomethane cis[24] CF3NNCF3 −40 −127 166 73513-59-4
Phosphoryl fluoride POF3 −39.7 sub −39.1 triple 104 13478-20-1
Chloropentafluoroethane CF3CClF2 −39.1 −99 135.5 76-15-3
Tetrafluoro(trifluoromethyl)phosphorane[25] CF3PF4 −39 −113 176 1184-81-2
tetrafluorophosphorane[26] PHF4 −39.0 −100 108 13659-66-0
Tellurium hexafluoride TeF6 −38.9 −37.6 triple 242 7783-80-4
Vinyldifluoroborane[27] CH2=CHBF2 −38.8 −133.4 76
(Trifluoromethyl)silane CF3SiH3 −38.3 −124 100 10112-11-5
Heptafluoroethanamine[3] C2F5NF2 −38.1 −183 171 354-80-3
Tetrafluoroallene[28] CF2=C=CF2 −38 112 461-68-7
Hexafluorooxetane[29] C3F6O −38 166 425-82-1
Trifluoromethanethiol[30] CF3SH −37.99 −157.11 102 1493-15-8
Fluoroethane CH3CH2F −37.7 −143.2 48 353-36-6
Bis(trifluoromethyl)peroxide CF3OOCF3 −37 170 927-84-4
Pentafluoropropanenitrile[31] C2F5CN −37 145 422-04-8
Perfluorodimethylamine[32] (CF3)2NF −37 171 359-62-6
Perfluoropropane C3F8 −36.8 −147.7 188 76-19-7
Germanium(IV) fluoride GeF4 −36.5 −15 triple 149 7783-58-6
Cyclopropene C3H4 −36 40 2781-85-3
Trifluoromethyl fluoroformate[33] CF3OC(O)F −36 −120 132 3299-24-9
Trifluoromethyl isocyanate[34] CF3NCO −36 111 460-49-1
Tetrafluoro-1,2-diazetidine C2F4N2H2 −36 130
Hydrogen iodide HI −35.5 −50.76 128 10034-85-2
Sulfur fluoride hypofluorite SOF6 −35.1 −86 162 15179-32-5
Trifluoromethyl difluoromethyl ether CF3OCHF2 −35.0 −157 136 3822-68-2
Propadiene CH2=C=CH2 −34.8 −136 40 463-49-0
Chlorine Cl2 −34.04 −101.5 71 7782-50-5
Trifluoromethyl fluoroformate[3][35] CF3OC(O)F −34 132 3299-24-9
Tetrafluorodiborane B2F4 −34 −56 98 13965-73-6
Ammonia NH3 −33.33 −77.73 17 7664-41-7
Trifluoronitromethane[36] CF3NO2 −32 115 335-02-4
Dichlorodifluorosilane SiCl2F2 −32 −44 137 18356-71-3
(Difluoroamino)difluoroacetonitrile[37] NF2CF2CN −32 128 5131-88-4
Hexafluoromethanediamine[3][38] (NF2)2CF2 −31.9 −161.9 154 4394-93-8
Bis(trifluoromethyl)diazene trans[3] CF3NNCF3 −31.1 166 372-63-4
Cyclopropane C3H6 −31 −127.6 42 75-19-4
Chlorosilane SiH3Cl −30.4 −118 66.5 13465-78-6
Perfluoropropene CF2=CFCF3 −30.2 −156.6 150 116-15-4
Chloroacetylene HCCCl −30 −126 60.5 593-63-5
Methyltrifluorosilane CH3SiF3 −30 −73 100 373-74-0
Fluorine azide[39] FN3 −30 −139 61.019 14986-60-8
Dichlorodifluoromethane CCl2F2 −29.8 −157.7 121 75-71-8
2,3,3,3-Tetrafluoropropene[40] CF3CF=CH2 −29.5 −152.2 114 754-12-1
Tetrafluorodiaziridine[3] CF4N2 −29 116 17224-09-8
fluoroxypentafluoroselenium[41] F5SeOF −29 209 [42]
Perfluorooxetane C3OF6 −28.6 −117 166 425-82-1
Chlorotrifluoroethene CClF=CF2 −28.3 −158.14 116.5 79-38-9
Methyldifluorophosphine CH3PF2 −28 −110 84 753-59-3
Perfluoroacetone CF3COCF3 −27.4 −125.45 166 684-16-2
Trifluoro(trifluoromethyl)oxirane C2OF3CF3 −27.4 −144 166 428-59-1
Thiazyl trifluoride N≡SF3 −27.1 −72.6 103 15930-75-3
Trifluoroacetyl chloride CF3COCl −27 −146 132.5 354-32-5
3,3,3-Trifluoropropene CF3CH=CH2 −27 96 677-21-4
Phosphonium chloride PH4Cl −27 sub 70.5 24567-53-1
Formyl fluoride HCOF −26.5 −142.2 48 1493-02-3
1,1,1,2-Tetrafluoroethane CF3CH2F −26.1 −103.296 102 811-97-2
Trifluoromethyl trifluorovinyl ether[3] CF3OCF=CF2 −26 166 5930-63-2
Methyl trifluoromethyl ether CF3OCH3 −25.2 −149.1 100 421-14-7
Bis(trifluoromethyl)nitroxide[43] (CF3)2NO −25 −70 168 2154-71-4
Sulfur cyanide pentafluoride[44] SF5CN −25 −107 153 1512-13-6[45]
Dimethyl ether CH3OCH3 −24.8 −141.49 46 115-10-6
1,1,1,4,4,4-Hexafluoro-2-butyne CF3C≡CCF3 −24.6 −117.4 162 692-50-2
1-Chloro-1-fluoroethene[3] CClF=CH2 −24.1 80.5 2317-91-1
1,1-Difluoroethane CHF2CH3 −24.05 −118.6 66 75-37-6
2-Fluoropropene[46] CH3CF=CH2 −24 60 1184-60-7
Borirane C2H4BH −24 −129 40 39517-80-1
Chloromethane CH3Cl −23.8 −97.4 50.5 74-87-3
Trifluoronitrosoethylene[47] CF2=CFNO −23.7 111 2713-04-4
Pentafluoro(trifluoromethoxy)ethane[48] C2F5OCF3 −23.6 204 665-16-7
1,1-Difluorocyclopropane[49] CF2CH2CH2 −23.5 78 558-29-2
Propyne or methylacetylene CH3CCH −23.2 −103.0 40 74-99-7
Diazomethane CH3NNCH3 −23 −145 58 334-88-3
Methylgermane CH3GeH3 −23 −158 91 1449-65-6
Difluoramine NHF2 −23 −116 53 10405-27-3
Prop-1-en-1-one or methylketene CH3CH=CO −23 −80 56 6004-44-0
Vinylsilane CH2=CHSiH3 −22.8 58 7291-09-0
Trifluoroiodomethane CF3I −22.5 −110 196 2314-97-8
Ethynylsilane HC≡CSiH3 −22.5 56 1066-27-9
Hexafluoro-1,3-dioxolane[50] c-CF2OCF2OCF2- −22.1 182.02 21297-65-4
Chloromethane sulfonyl chloride[3] CH2ClS(O)(O)Cl −22 149 3518-65-8
Trifluoromethyl peroxychloride[3] CF3OOCl −22 −132 136.5 32755-26-3
Carbon oxyselenide COSe −21.7 −124.4 107 1603-84-5
Trifluoromethanesulfonyl fluoride CF3SOF −21.7 136 335-05-7
Chloryl trifluoride ClO2F3 −21.6 −81.2 124.5 38680-84-1
Carbonyl bromide fluoride COBrF −21 127 753-56-0
Bromopentafluoroethane C2BrF5 −21 199 354-55-2
Cyanogen NCCN −21 −27.83 52 460-19-5
Methyl silyl ether CH3OSiH3 −21 −98.5 62 2171-96-2
Carbonic bromide fluoride[3] CBrFO −20.6 127 753-56-0
Trifluoromethylsulfur pentafluoride[3] CF3SF5 −20.4 −87 196 373-80-8
Chlorotrifluorogermane GeClF3 −20.3 −66.2 165.5 14188-40-0
Trimethylborane (CH3)3B −20.2 −159.93 56 593-90-8
Dimethylsilane (CH3)2SiH2 −20 −150 60 1111-74-6
1,1,2,2-Tetrafluoroethane CHF2CHF2 −20 −89 66 359-35-3
Formaldehyde H2CO −19.1 −92 30 50-00-0
Hexafluorodisilane SiF3SiF3 −19.1 −18.7 triple 170 13830-68-7
Sulfur chloride pentafluoride SClF5 −19.05 −64 158.5 13780-57-9
1-Chloro-2,2-difluoroethene CHCl=CF2 −18.8 −138.5 98.5 359-10-4
1,1,1,2,2-Pentafluoropropane CF3CF2CH3 −18 133 1814-88-6
Difluoroamino sulfur pentafluoride[51] NF2SF5 −17.5 179 13693-10-2
Stibine SbH3 −17 −88 125 7803-52-3
1,1,2,2,3,3,3-Heptafluoropropane[52] CF2HCF2CF3 −17 −148.5 170 2252-84-8
1,1,1,2,3,3,3-Heptafluoropropane CF3CHFCF3 −16.34 −126.8 170 431-89-0
Phosphorus(III) bromide difluoride PBrF2 −16.1 −133.8 149 15597-40-7
Methylphosphine CH3PH2 −16 48 593-54-4
N,N-Difluoromethanamine[3][53] CH3NF2 −16 −114.8 67 753-58-2
Fluorine perchlorate FOClO3 −16 −167.3 118.5 10049-03-3
Bis(trifluoromethyl) trioxide[54] CF3OOOCF3 −16 −138 186
1,3,3,3-Tetrafluoropropene[3] CF3CH=CHF −16 −104.53 114 1645-83-6
1-Trifluoromethyl-1,2,2-trifluorocyclopropane[49] CF3CH2F3 −15.8 152
Disiloxane (SiH3)2O −15.2 −144 78 13597-73-4
cis-1-Fluoropropene CH3CH=CHF −15 60 19184-10-2
trans-1-Fluoropropene CH3CH=CHF −15? 60 20327-65-5
Nitryl chloride NO2Cl −15 −145 81.5 13444-90-1
Chlorazide ClN3 −15 −100 77.47 13973-88-1
Disilane Si2H6 −14.8 −129.4 62 1590-87-0
Bromodifluoromethane CHBrF2 −14.6 −145 131 1511-62-2
Chloroethene CH2=CHCl −13.8 −153.84 62.5 75-01-4
Monoethylsilane[55] CH3CH2SiH3 −13.7 −180 60 2814-79-1
Chlorine pentafluoride ClF5 −13.1 −103 130.5 13637-63-3
1,1,1-Trifluoropropane CF3CH2CH3 −13 98 421-07-8
1-Chloro-1,1,2,2-tetrafluoroethane CClF2CHF2 −13 −117 135.5 354-25-6
Carboimidic difluoride CF2NH −13 dec −90 65 2712-98-3
Plumbane PbH4 −13 211 15875-18-0
Methyl nitrite CH3NO2 −12 −16 61 624-91-9
Trifluoromethylarsine[56] CF3AsH2 −12 146 420-42-8
1-Chloro-1,2,2,2-tetrafluoroethane CHClFCF3 −11.96 −199.15 136.5 2837-89-0
Isobutane (CH3)2CHCH2CH3 −11.7 −159.42 58 75-28-5
Trifluoromethoxy sulfur pentafluoride[57] CF3OSF5 −11 −143 212 1873-23-0
Thiothionyl fluoride SSF2 −10.6 −164.6 102 101947-30-2
Sulfur dioxide SO2 −10.05 −75.5 64 7446-09-5
2-Fluoropropane CH3CHFCH3 −10 62 420-26-8
Pentafluoroethyl hypochlorite[58] C2F5OCl −10± 170.5 22675-67-8
Fluoroformyl sulfurpentafluoride[59] SF5C(O)F −10 174
Trifluoromethyl fluoroformyl peroxide[60] CF3OOC(O)F −10~ 148 16118-40-4
Perfluorodimethoxymethane CF3OCF2OCF3 −10 −161 220 53772-78-4
1-Chloro-1,1-difluoroethane CClF2CH3 −9.6 −130.8 100.5 75-68-3
Chlorofluoromethane CH2ClF −9.1 −133.0 68.5 593-70-4
Pentafluoroethyl isocyanate[61] C2F5NCO −9 157 356-74-1
Bis(trifluoromethyl)chloramine[62] (CF3)2NCl −9 187.5
Selenium dioxydifluoride SeO2F2 −8.4 −99.5 149 14984-81-7
Fluoro(trifluoro-methyl)diazine[3] CF4N2O −7.63 132 815-10-1
Isobutene (CH3)2C=CH2 −7.0 −140.7 56 115-11-7
3-Fluoropropene CH2=CHCH2F −7 60 818-92-8
Bis(trifluromethyl)amine[3] (CF3)2NH −7 153 371-77-7
Ethoxytrifluorosilane[63] CH3H2OSiF3 −7 −122 118 460-55-9
Trifluoromethylsulfur trifluoride[64] CF3SF3 −7 −110 158 374-10-7
Perfluoro-2-methyl-1,2-oxazetidine[65] (CF3-N)CF2CF2O −6.8 199
Tris(trifluoromethyl)-amine[32] (CF3)3N −6.5 221 432-03-1
Methylamine CH3NH2 −6.4 −93.42 31 74-89-5
1-Butene CH2=CHCH2CH3 −6.3 −185.33 56 106-98-9
Diphosphorus tetrafluoride P2F4 −6.2 −86.5 138 13824-74-3
Chloryl fluoride ClO2F −6 −115 86.5 13637-83-7
Trifluoromethyl iminosulfur difluoride[66] CF3N=SF2 −6 153 1512-14-7
Perfluorocyclobutane -CF2CF2CF2CF2- −5.91 −40.16 200 115-25-3
Perfluoro-2-butene CF3CCF=CF3 −5.9 200 360-89-4 trans
Nitrosyl chloride ONCl −5.55 −59.4 65.5 2696-92-6
Difluorocarbamoylchloride CClF2NO −5.5 115.5 16847-30-6
Hexafluoro 1,2-dioxolane[67] -CF2CF2CF2OO- −5 −115.5 182.02
1,3-Butadiene CH2=CHCH=CH2 −4.6 −108.9 54 106-99-0
Ethyltrifluorosilane[68] CH3CH2SiF3 −4.4 −105 114 353-89-9
Difluoro-N-fluoromethanimine F2C=NF −4 83 338-66-9
1,1-Dimethyldiborane (CH3)2B(μ-H)2BH2 −4 −150.2 56 16924-32-6
Bromochlorodifluoromethane CF2ClBr −3.7 −159.5 165.5 353-59-3
N-Nitroso-bis(trifluoromethyl)amine[69] ONN(CF3)2 −3.5 182
Trifluoromethyl 1,1,2,2-tetrafluoroethyl ether[50] CF3OCF2CF2H −3.3 −141 186 2356-61-8
1-Fluoropropane[3] CH2FCH2CH3 −3.2 −159 62 460-13-9
3-Fluoropropene[46] CH2CHCH2F −3 60 818-92-8
Dimethylperoxide CH3OOCH3 −3 −100 62 690-02-8
Trifluoromethyl thionitrite[70] CF3SNO −3 131
Dichlorodifluorogermane GeCl2F2 −2.8 −51.8 182 24422-21-7
Bromotrifluoroethene CBrF=CF2 −2.5 161 598-73-2
Trifluoromethane sulfinyl fluoride[3] CF3SOF −2.5 136 812-12-4
Sárfhluarabútán C4F10 −2.1 −129 238 355-25-9
Teallúiríd hidrigine H2Te −2 −49 130 7783-09-7
1-Chloroheptafluoropropane[71] CF3CF2CF2Cl −2 204.5 422-86-6
2-Chloroheptafluoropropane[71] CF3CFClCF3 −2 204.5 76-18-6
Bis(trifluoromethyl)selenium[72] (CF3)2Se −2 217 371-79-9
Trifluoromethyl sulfinyl fluoride[64] CF3S(O)F −1.6 136 812-12-4
1,1,1,2,2,3-Hexafluoropropane CF3CF2CFH2 −1.44 −98.38 152 677-56-5
1,1,1,3,3,3-Hexafluoropropane CF3CH2CF3 −1.4 −93.6 152 690-39-1
Pentafluoroguanidine[73] CF5N3 −1 149 10051-06-6
1,1,2,2-Tetrafluoropropane[74] CHF2CF2CH3 −0.8 −121.1 116 40723-63-5
Heptafluoronitrosopropane[18] C3F7NO −0.7 199 354-72-3
Trifluoromethanesulfenylchloride[3] CF3SCl −0.6 136.5 421-17-0
1,1,1,2-Tetrafluoropropane CF3CHFCH3 −1-0 116 421-48-7
1,1,2,2,3,3-Hexafluoropropane[3] CHF2CF2CHF2 −0.3 −98.38 152 680-00-2
Bútán C4H10 0 −140 58 106-97-8
2,2-Difluoropropane CH3CF2CH3 0 −104.8 80 420-45-1
[Difluoropropane]] C4F10 0 238 354-92-7
Nitrosyl bromide NOBr 0 −56 110 13444-87-6
Teatrocsaíd xeanóin XeO4 0 dec −35.9 195 12340-14-6
Trifluoromethylsulfonyl hypofluorite[75] CF3SO2OF 0 −87 168
Trifluoromethyl chloroformate[76] CF3OC(O)Cl 0 148.5 23213-83-4
Decafluorodiethyl ether perfluoro ether[77] CF3CF2OCF2CF3 0 254 358-21-4
Perfluorocyclobutanone[78] -CF2CF2CF2C(O)- 0 178 699-35-4
Trifluoromethyl peroxonitrate[3] CF3OON2 0.4 129 50311-48-3
Thiazyl fluoride[79] NSF 0.4 −89 65.07 18820-63-8
Sárfhluaraiteteitrihidreafúrán -OCF2CF2CF2CF2- 0.6 −85 216 773-14-8
Tetrafluoro(trifluoromethylimino)-λ6-sulfane[80] F4S=NCF3 0.75±0.25 191
trans-2-Butene CH3CH=CHCH3 0.9 −43.3 56 624-64-6
Meitilcioglapróipéin CH3CHCH2CH2 1 −177.2 56 594-11-6
Bis(trifluoromethyl)phosphine[81] (CF3)2PH 1 170
Oxalyl fluoride[13] CFOCFO 1±1 −12.42 94 359-40-0
Methylstannane CH3SnH3 1.4 137 1631-78-3
tras-Démheitildéimíd = asómeatán CH3N=NCH3 1.5 −78 58 503-28-6
Bromosilane SiH3Br 1.9 −94 111 13465-73-1
Airsínmeitile CH3AsH2 2 −143 92 593-52-2
Heicseafluaraicioglabúitéin C4F6 2 −60 162 697-11-0
Aonocsaíd chlóirín Cl2O 2.2 −120.6 87 7791-21-1
Cioglabúitéin C4H6 2.5 54 822-35-5
Difluorodimethylsilane (CH3)2SiF2 2.5 −87.5 96 353-66-2
1,1,1-Trifluoroazomethane[3] CF3NNCH3 2.5 112 690-21-1
dichorotrifluorophosphorane[26] PCl2F3 2.5 −124 159 13659-65-9
Trímheitiolaimín (CH3)3N 2.8 −117.1 59 75-50-3
1,1-Dichloro-1,2,2,2-tetrafluoroethane CCl2CF3 3 −56.6 152 374-07-2
Sulfur bromide pentafluoride SBrF5 3.1 −79 207 15607-89-3
1,1,2-trifluoroethane CHF2CH2F 3.5 −84 84 430-66-0
1,2-déchlóraí-1,1,2,2-teitreafluaireatán CClF2CClF2 3.6 −92.52 171 76-14-2
cios-2-Búitéin CH3CH=CHCH3 3.72 −138.9 56 590-18-1
Phosphorus dihydride trifluoride[26] PH2F3 3.9 −52 90
Brómaimeatán CH3Br 4 −93.66 95 74-83-9
1,2-Dimethyldiborane [(CH3)BH2]2 4 −124.9 56 17156-88-6
Selenium chloride pentafluoride SeClF5 4.5 −19 209.5 34979-62-9
1,1,4,4-Tetrafluoro-1,3-butadiene[82] CF2=CFCF=CF2 4.5± 162 407-70-5
Trifluoromethyl phosphorodifluoridate[75] CF3OP(O)F2 4.6 −96.2 170 39125-43-4
Bromoacetylene C2HBr 4.7 105 593-61-3
Iodine heptafluoride IF7 4.8 6.5 triple 250 16921-96-3
Dimethylchloroborane[3] (CH3)2BCl 4.9 −39.9 76.5 1803-36-7
Perfluoro-1-butene[3] CF3CF2CF=CF2 5 200 357-26-6
Sulfur pentafluoride cyanate[83] F5SOCN 5 −60 169
Pentafluorosulfanyl cyanate[80] F5SOCN 5-5.5 169
1,1,2,3,4,4-Hexafluoro-1,3-butadiene CF2CFCFCF2 5.4 −132 162 685-63-2
Bis(difluoromethyl) ether CHF2OCHF2 5.5 118 1691-17-4
Methyl pentafluoroethyl ether CH3OC2F5 5.6 140 22410-44-2
Tris(difluoroamine)fluoromethane[3] (NF2)3CF 5.6 −136.9 187 14362-68-6
Perfluoro ethyl methyl ether C2F5OCF3 5.61 204
1-Bromo-2,2-difluoro-ethylene[84] CHBr=CF2 5.7 143
Methanethiol[3] CH3SH 5.95 −123 48 74-93-1
1-Buten-3-yne CH2CHC≡CH 6 54 689-97-4
Éitear meitile eitile CH3OC2H5 6 −113 60 540-67-0
Éitear vinilmeitile? CH3OCH=CH2 6 −122 58 107-25-5
1,1,1-Trifhluara--2-clóireatán ? CF3CH2Cl 6.1 −105.5 118.5 75-88-7
1,1,1,2,3,3-Hexafluoropropane CF3CH2CF3 6.2 152 431-63-0
Phosphorothioic chloride difluoride PSClF2 6.3 −155.2 136.5 2524-02-9
Perfluoro-2-methoxypropionylfluoride[78] CF3OCF(CF3)C(O)F 5-8 232
Trimethylsilane (CH3)3SiH 6.7 −153.9 74 993-07-7
Carbon suboxide OCCCO 6.8 −111.3 68 504-64-3
2-Chloropentafluoropropene[52] CF3CCl=CF2 6.8 166.5 2804-50-4
dimethylgermane[85] CH3GeH2CH3 7.0 104.72 1449-64-5
Perfluoroisobutene (CF3)2C=CF2 7 −130 200 382-21-8
Pentafluoroethyl trifluorovinyl ether CF3CF2OCFCF2 7 216 10493-43-3
1,1-Difluoropropane CHF2CH2CH3 7-8 80 430-61-5
1,1,1,2,4,4,4-Heptafluoro-2-butene[65] CF3CF=CHCF3 7-8 182
Chloromethylsilane CH3ClSi 7 −135 78.5 993-00-0
Fluoromethyldifluoroborane[86][87] CH2FBF2 7 −47 82
Nitryl cyanide[88] NCNO2 7 −85
Phosphorus(V) dichloride trifluoride PCl2F3 7.1 −125 159 13454-99-4
Sulfuryl chloride fluoride SO2ClF 7.1 −124.7 118.5 13637-84-8
Dimethylamine (CH3)2NH 7.3 −93 45 124-40-3
3-Chloropentafluoropropene[52] CF2ClCF=CF2 7.4 166.5 79-47-0
Carbonyl chloride (Phosgene) COCl2 7.5 −127.77 99 75-44-5
Chloropentafluoroacetone CClF2COCF3 7.8 −133 182.5 79-53-8
1-Butyne CH3CH2C≡CH 8.08 −125.7 54 107-00-6
Dichlorosilane SiH2Cl2 8.3 −122 101 4109-96-0
trans-1,1,1,4,4,4-hexafluoro-2-butene[89] CF3CH=CHCF3 8.5 407-60-3
2-Bromo-1,1,1,2-tetrafluoroethane[65] CF3CHFBr 8.65 181
Methyl chlorosilane[3] CH3SiH2Cl 8.7 −134.1 80.5 993-00-0
Pentafluorosulfanyl hypochloriteTeimpléad:Citation needed SF5OCl 8.9 178.5
Dichlorofluoromethane CHCl2F 8.92 −135 103 75-43-4
ethylgermane[90] CH3CH2GeH3 9.2 104.66
Neopentane (CH3)4C 9.5 −16.5 72 463-82-1
Trifluoromethylperchlorate CF3OClO3 9.5 168.5 52003-45-9
1-Chloro-2-fluoroethene[3] CClF=CH2 9.8 80.5 460-16-2
1,3-Butadiyne HC≡CC≡CH 10 −35 50 460-12-8
N-Nitroso-O,N-bis(trifluoromethyl)-hydroxylamine or
O-Nitroso-bis(trifluoromethy1)hydroxylamine[91][92] 		CF3(CF3O)NNO or
(CF3)2NONO 		10 198 367-54-4
Ethylene oxide CH2OCH2 10.4 −112.46 44 75-21-8
1,2-Difluoroethane[3] CH2FCH2F 10.5 −118.6 66 624-72-6
1,2-Butadiene = methylallene CH3CH=C=CH2 11 −136.20 54 590-19-2
Dichloromethylborane CH3BCl2 11 97 7318-78-7
Chlorine dioxide ClO2 11 −59 103 10049-04-4
2-Chloro-2,3,3,3-tetrafluoropropanoyl fluoride[93] CF3CFClC(O)F 11 182.5 28627-00-1
Methyl trifluorovinyl ether[94] CH3OCF=CF2 11 112 3823-94-7
Trifluoromethyl hydroperoxide[3][95] CF3OOH 11.3 102 16156-36-8
Methyl trifluoromethyl sulfide[72] CH3SCF3 11.5 116 421-16-9
Chlorine trifluoride ClF3 11.75 −76.34 128 7790-91-2
1-bromoheptafluoropropane[71] CF3CF2CF2Br 12 249 422-85-5
Tert-butylfluoride[96] (CH3)3CF 12 76 353-61-7
2-Fluoro-2-methylpropane CH3(CH3)CFCH3 12.1 76 353-61-7
Trichlorofluorosilane SiCl3F 12.25 153.5 14965-52-7
Chloroethane CH3CH2Cl 12.27 −138 64.5 75-00-3
Pentafluoroiodoethane[97] CF3CF2I 12.5 −92 246 354-64-3
Cyclobutane C4H8 12.5 −90.7 56 287-23-0
1,1-difluoro-N-(pentafluoro-λ6-sulfanyl)methanimine[80] F5SN=CF2 12.5±0.5 191
2-diazo-1,1,1,3,3,3-hexafluoropropane[98] (CF3)2CN2 12.5±0.5 684-23-1
Silylphosphine[99] SiH3PH2 12.7 68 14616-47-8
Cyanogen chloride ClCN 13 −6.55 61.5 506-77-4
trans-1-Bromo-1,2-difluoroethylene[84] CBrF=CFH 13 143 358-99-6
Trifluoromethyl phosphine[3] CF3PH2 13.1 102 420-52-0
2,2,2-Trifluorodiazoethane[100] CF3CHNN 13.2 91 371-67-5
2-Chloro-1,1,1,2-tetrafluoropropane HCFC-244bb[101] CF3CClFCH3 13.23 150.5 421-73-8
Pentafluoroethyl sulfur pentafluoride[102] C2F5SF5 13.5 246
Phosphorus(III) dichloride fluoride PCl2F 13.85 −144 121 15597-63-4
2-Chloro-1,1,1,3,3,3-hexafluoropropane[52] CF3CHClCF3 14 −120.8 186.5 51346-64-6
Difluoro(difluorochloromethyl)amine CClF2NF2 14.14 137.5 13880-71-2
Nitrosyl bromide ONBr 14.5 110 13444-87-6
Hexafluoroisobutylene[3] (CF3)2C=CH2 14.5 164 382-10-5
N,N-Difluoroethylamine[53] CH3CH2NF2 14.9 −150.3 81 758-18-9
2-(Pentafluorothio)-3,3-difluorooxaziridine[103] SF5(-NCF2O-) 14.0 207 73002-62-7
Disulfur difluoride FSSF 15 −133 102 13709-35-8
1,1,1,3,3-Pentafluoropropane[3] CF3CH2CHF2 15.14 −102.10 134 460-73-1
1,1,1,2,2,3,3,4,4-Nonafluorobutane[3] CF3CF2CF2CF2H 12 220 375-17-7
Trifluoromethyl phosphorodifluoroperoxoate[75] CF3OOP(O)F2 15.5 −88.6 167 39125-42-3
(Trifluoroacetyl)sulfur pentafluoride[59] CF3C(O)SF5 15.6 −112 224 82390-51-0
Bróimíd vinile CH2=CHBr 15.8 −137.8 107 593-60-2
Bis(fluorocarbonyl) peroxide[104][13] CF(O)OOCFO 15.9 −42.5 126 692-74-0
1-Chloro-1,1,2-trifluoroethane CClF2CH2F 16 118.5 421-04-5
cis-1-Bromo-1,2-difluoroethylene[84] CBrF=CHF 16 143
1-Fluoro-2-methylpropane[96] CH2FCHCH3CH3 16 76 359-00-2
Difluoromethyl 1,1,2-trifluoroethyl ether CHF2OCF2CH2F 16.14 150 69948-24-9
1-Chloro-1-fluoroethane[3] CHClFCH3 16.15 82.5 1615-75-4
Fluorotrimethylsilane (CH3)3SiF 16.4 −74.3 92 420-56-4
Bis(trifluoromethyl)nitramine[62] (CF3)2NNO2 16.4 198
Hexafluoroacetone imine[105] CF3C(=NH)CF3 16.5± −47 165 1645-75-6
Dichloro(trifluoromethyl)amine[3] CF3NCl2 16.6 154 13880-73-4
Eitiolaimín CH3CH2NH2 16.6 −81 45 75-04-7
1,1,1-Trifluorobutane[106] CF3CH2CH2CH3 16.74 −114.79 112 460-34-4
Bismuth hydride BiH3 17 −67 212 18288-22-7
2,2,3,3-Tetrafluorobutane[65] CH3CF2CF2CH3 17 130
heicseafluairíd (VI) tungstain WF6 17.1 1.9 294 7783-82-6
1-Chloro-1,2,2-trifluoroethane CHClFCHF2 17.3 99.5 431-07-2
Bis (trifluoromethyl) carbamyl fluoride (CF3)2NC(O)F 17.5±2.5 199
Nítrít eitile C2H5NO2 17.5 75 109-95-5
Tetraborane(10) B4H10 18 −120 54 18283-93-7
trifluoro-(sulfinylamino)methane[107] CF3N=S=O 18 131 10564-49-5
F-2,3-dihydro-1,4-dioxin[108] -CF2CF2OCF=CFO- 18.5 158
Brómafluaraimeatán CH2BrF 19 (CRC=23) 113 373-52-4
Bis(trifluoromethyl)arsine[56] (CF3)2AsH 19 214
1,1-Dichloro-2,2-difluoroethene CCl2=CF2 19 −116 135 79-35-6
Perfluorovinylsulphur pentafluoride[109] CF2=CFSF5 19 208 1186-51-2
Fluoroformic acid anhydride[110] FC(O)OC(O)F 19.2 −46.2 110 177036-04-3
Trifluorovinyl isocyanate[111] CF2=CFNCO 19.5 123 41594-57-4
Fluairíd hidrigine HF 20 −83.36 20 7664-39-3
Bromine monofluoride BrF 20 dec −33 99 13863-59-7
Perbromyl fluoride BrO3F 20 dec −110 147 25251-03-0
1-Chloro-1,1,2,2-tetrafluoropropane[112] CF2ClCF2CH3 20 150.5 421-75-0
Perfluorooxaspiro[2.3]hexane[78] C5F8O 18-21 228
pentafluoroethylsulfinyl fluoride[64] C2F5S(O)F 20 186 20621-31-2
3-Methyl-1-butene CH2=CHCH(CH3)2 20.1 −168.41 70 563-45-1
Aicéataildéad CH3CHO 20.2 −123.37 44 75-07-0
Chlorotetrafluoro(trifluoromethyl)sulfur CF3SClF4 20.2 212.5 42179-04-4
trans-Bis(trifluoromethyl)sulfur tetrafluoride[113] CF3SF4CF3 20.5 246 42179-02-2
Decafluorocyclopentane[3] C5F10 20.5 250 376-77-2
1,1-Dimethylcyclopropane (CH3)2CCH2CH2 21 −109.0 70 1630-94-0
Acetyl fluoride CH3C(O)F 21 −84 62 557-99-3
Perfluoro-N-methyloxazolidine CF3-NCF2OCF2CF2- 21 237
Bis(trifluoromethyl)cyanoamine[62] (CF3)2NCN 21 178
Bis(trifluoromethyl)sulfur difluoride[72] (CF3)2SF2 21 198 30341-38-9
Perfluoroethyldimethylamine[32] C2F5(CF3)2N 21±1 271 815-28-1
cis-1,2-Dichloro-1,2-difluoroethene CClF=CClF 21.1 −119.6 133 598-88-9
Trifluoromethyl trifluoromethanesulfonate[114] CF3SO2OCF3 21.2 −108.2 218 3582-05-6
Nitrogen tetroxide N2O4 21.15 −9.3 92 10544-72-6
Difluoroiodomethane CHF2I 21.5 −122 178 1493-03-4
Trifluoromethylcyclopropane[49] C5H6F3CH3 21.6 110 381-74-8
1,1,1-Trifluoroacetone CF3C(O)CH3 21.9 −78 112 421-50-1
trans-1,2-Dichloro-1,2-difluoroethene CClF=CClF 22 −93.3 133 27156-03-2
Heptafluoroisopropyl hypochlorite[58] (CF3)2CFOCl 22 220.5 22675-68-9
Perfluoroazoethane[34] C2F5NNC2F5 22 266
1,2,2-Trifluoropropane[115] CH2FCF2CH3 22 98 811-94-9
Bis(trifluoromethyl)bromamine[62] (CF3)2NBr 22 232
Bis(trifluoromethyl)sulfde[116] (CF3)2S 22.2 170 371-78-8
1,1,1,3,3-Pentafluorobutane CF3CH3CF2CH3 22.6 −34.1 149 406-58-6
octafluoro-1,4-dioxane[117] (-CF2CF2OCF2CF2O-) 22.75±0.25 232 32981-22-9
Isicianáit HNCO 23 −86 43 420-05-3
2-Chloropropene CH3CCl=CH2 23 −137.4 76.5 557-98-2
1,2,2,2-Tetrafluoroethyl difluoromethyl ether CF3CHFOCHF2 23 168 57041-67-5
1,1,1,2,3-Pentafluoropropane[118] CF3CHFCH2F 23 134 431-31-2
2,2,3,3,4,4,5-Heptafluoro oxolane[119] -CF2CF2CF2CHFO- 23 179
Pentafluoroethyl iminosulfur difluoride[66] CF3CF2N=SF2 23±1 203
Methoxyacetylene[120] CH3OC≡CH 23±0.5 56 6443-91-0
Carbonyl fluoride iodide COFI 23.4 174 1495-48-3
1,2,2,2-Tetrafluoroethyl difluoromethyl ether[3] CF3CHFOCHF2 23.4 168 57041-67-5
Propylsilane[55] CH3CH2CH2SiH3 23.5± 78 13154-66-0
Trichlorofluoromethane CCl3F 23.77 −110.48 137.5 75-69-4
Formic anhydride C2O3H2 24/20 mmHg 74 1558-67-4
1-Chloro-1,3,3,3-tetrafluoropropene[52] CF3CH=CFCl 24 148.5 460-71-9
1,1,2,2-Tetrafluoro-1-nitro-2-nitrosoethane[121] NO2CF2CF2NO 24.2 176 679-08-3
Germyl methyl ether[122] GeH3OCH3 24.3 5910-93-0
Dibromodifluoromethane[3] CBr2F2 24.45 −141.5 210 75-61-6
Heptafluoro-N-propyl isocyanate[18] C3F7NCO 24.5 211 87050-96-2
Hexafluorobut-2-yne[65] CF3C≡CCF3 24.6 −117.4 162 692-50-2
1,1,1,4,4,4-Hexafluorobutane[123] CF3CH2CH2CF3 24.6 407-59-0
Chloroheptafluorocyclobutane C4ClF7 25 −39.1 216.5 377-41-3
Dimethylphosphine (CH3)2PH 25 62 676-59-5
Ethyl phosphine[124] CH3CH2PH2 25 62 593-68-0
Octafluorocyclopentene[125] C5F8 25 212 559-40-0
2-Fluorobutane[126] CH3CHFCH2CH3 25 −121 76 359-01-3
  1. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."" (en).
  2. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."" (en).
  3. ↑ 3.00 3.01 3.02 3.03 3.04 3.05 3.06 3.07 3.08 3.09 3.10 3.11 3.12 3.13 3.14 3.15 3.16 3.17 3.18 3.19 3.20 3.21 3.22 3.23 3.24 3.25 3.26 3.27 3.28 3.29 3.30 3.31 3.32 3.33 3.34 3.35 3.36 3.37 3.38 3.39 3.40 3.41 3.42 3.43 "The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals: Physical Properties for More Than 54,000 Organic and Inorganic Chemical Compounds, Coverage for C1 to C100 Organics and Ac to Zr Inorganics" (as en) (2015). Gulf Professional Publishing. 
  4. ↑ Journal of Heterocyclic Chemistry. - 1964. - Vol. 1, No. 1. - pp. 59-60
  5. ↑ "Phosphorus: Chemistry, Biochemistry and Technology, Sixth Edition" (as en) (2016). CRC Press. 
  6. ↑ "Fluoroperoxytrifluoromethane, CF3OOF. Preparation from trifluoromethyl hydroperoxide and fluorine in the presence of cesium fluoride" (January 1972). Inorganic Chemistry 11 (1): 193–195. doi:10.1021/ic50107a047. 
  7. ↑ Journal of Fluorine Chemistry. - 2013. - Vol. 155. - pp. 29-31 full citation needed
  8. ↑ "846. Thiocarbonyl fluoride" (1962). Journal of the Chemical Society (Resumed): 4361. doi:10.1039/JR9620004361. 
  9. ↑ "Difluorocyanamide" (August 1966). Inorganic Chemistry 5 (8): 1455–1457. doi:10.1021/ic50042a040. 
  10. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."" (en).
  11. ↑ Advances in Inorganic Chemistry and Radiochemistry. - 1961. - Vol. 3. - p. 406
  12. ↑ "Difluoroaminooxyperfluoromethane, CF3ONF2" (October 1965). Inorganic Chemistry 4 (10): 1516–1517. doi:10.1021/ic50032a045. 
  13. ↑ 13.0 13.1 13.2 "Handbook of the Thermodynamics of Organic Compounds" (as en) (2012). Springer Science & Business Media. 
  14. ↑ "Difluoraminocarbonyl Fluoride" (October 1965). Inorganic Chemistry 4 (10): 1497–1498. doi:10.1021/ic50032a034. 
  15. ↑ Landolt-Bornstein Numerical Data and Functional Relationships in Science and Technology. Group IV, Volume 20: Vapor Pressure of Chemicals. Subvolume A: Vapor Pressure and Antoine Constants for Hydrocarbons, and Sulfur, Selenium, Tellurium, and Halogen Containing Organic Compounds. - 1999. - p. 197
  16. ↑ Journal of the American Chemical Society. - 1965. - Vol. 87, No. 2. - pp. 231-233
  17. ↑ Advances in Inorganic Chemistry and Radiochemistry. - 1961. - Vol. 3. - p. 226
  18. ↑ 18.0 18.1 18.2 "663. Perfluoroalkyl derivatives of nitrogen. Part III. Heptafluoronitrosopropane, perfluoro-2-n-propyl-1 : 2-oxazetidine, perfluoro-(methylene-n-propylamine), and related compounds" (1956). Journal of the Chemical Society (Resumed): 3416. doi:10.1039/JR9560003416. 
  19. ↑ "Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 18: Four Carbon-Heteroatom Bonds" (as en) (2014). Georg Thieme Verlag. 
  20. ↑ Bivens D.B., Minor B.H. Fluoroethers and other next generation fluids / International Journal of Refrigeration. - 1998. - Vol. 21, No. 7. - p. 570
  21. ↑ Advances in Inorganic Chemistry and Radiochemistry. - 1970. - Vol. 13. - p. 368
  22. ↑ Bivens D.B., Minor B.H. Fluoroethers and other next generation fluids / International Journal of Refrigeration. - 1998. - Vol. 21, No. 7. - p. 569
  23. ↑ Inorganic Chemistry. - 1972. - Vol. 11, No. 6. - p. 1259-1264
  24. ↑ "Die Fluorierung des Silbercyanids. (I.)" (as de) (4 March 1936). Berichte der Deutschen Chemischen Gesellschaft (A and B Series) 69 (3): 598–603. doi:10.1002/cber.19360690325. 
  25. ↑ Inorganic Chemistry. - 1963. - Vol. 2, No. 1. - p. 230
  26. ↑ 26.0 26.1 26.2 "Pentacoordinated Molecules. VIII. Preparation and Nuclear Magnetic Resonance Study of PH2F3 and PHF4" (December 1966). Inorganic Chemistry 5 (12): 2146–2150. doi:10.1021/ic50046a015. 
  27. ↑ Journal of the American Chemical Society. - 1960. - Vol. 82, No. 24. - p. 6219
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  29. ↑ Bivens D.B., Minor B.H. Fluoroethers and other next generation fluids / International Journal of Refrigeration. - 1998. - Vol. 21, No. 7. - p. 568
  30. ↑ "Thermodynamic Properties of Trifluoromethanethiol from 12°K to Its Boiling Point. Entropy from Molecular and Spectroscopic Data" (March 1960). The Journal of Chemical Physics 32 (3): 805–809. doi:10.1063/1.1730801. Bibcode: 1960JChPh..32..805D. 
  31. ↑ Journal of the American Chemical Society. - 1959. - Vol. 81, No. 14. - p. 3602
  32. ↑ 32.0 32.1 32.2 "22. Perfluoro-tert.-amines" (as en) (1951). Journal of the Chemical Society (Resumed): 102. doi:10.1039/jr9510000102. ISSN 0368-1769. 
  33. ↑ "Trifluoromethyl fluoroformate" (1965). Chemical Communications (London) (12): 241. doi:10.1039/C19650000241. 
  34. ↑ 34.0 34.1 "The Synthesis and Chemistry of Fluoroazoalkanes" (June 1962). Journal of the American Chemical Society 84 (12): 2337–2343. doi:10.1021/ja00871a014. 
  35. ↑ US Patent 3226418
  36. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."".
  37. ↑ "Photochemical Fluorinations of C2N2 and RfN=-SF2 with N2F4" (August 1965). Inorganic Chemistry 4 (8): 1228–1230. doi:10.1021/ic50030a033. 
  38. ↑ "Separation of Tris(difluoroamino)fluoromethane and Bis(difluoroamino)fluoromethane with Crystalline Zeolites" (1 December 1969). Industrial & Engineering Chemistry Product Research and Development 8 (4): 443–445. doi:10.1021/i360032a024. 
  39. ↑ "Properties of triazadienyl fluoride, N3F" (1987-07-01). Inorganic Chemistry 26 (13): 2137–2140. doi:10.1021/ic00260a025. ISSN 0020-1669. 
  40. ↑ "Saturated Pressure Measurements of 2,3,3,3-Tetrafluoroprop-1-ene (R1234yf) for Reduced Temperatures Ranging from 0.67 to 0.93" (12 May 2011). Journal of Chemical & Engineering Data 56 (5): 2608–2612. doi:10.1021/je2000952. 
  41. ↑ "Reactions of fluoroxypentafluoroselenium" (June 1970). Inorganic Chemistry 9 (6): 1442–1445. doi:10.1021/ic50088a029. 
  42. ↑ "The Chemistry of Fluorine and Its Compounds" (as en) (2013). Elsevier. 
  43. ↑ "A New Stable Radical, Bis(trifluoromethyl) Nitroxide" (February 1965). Journal of the American Chemical Society 87 (4): 802–805. doi:10.1021/ja01082a019. 
  44. ↑ "Sulfur Cyanide Pentafluoride SF5 CN" (September 1989). Angewandte Chemie International Edition in English 28 (9): 1255–1256. doi:10.1002/anie.198912551. 
  45. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."". Landolt-Börnstein Substance/Property Index.[nasc briste go buan]
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  47. ↑ "279. Perfluoroalkyl derivatives of nitrogen. Part VIII. Trifluoronitrosoethylene and its polymers" (1960). Journal of the Chemical Society (Resumed): 1398. doi:10.1039/JR9600001398. 
  48. ↑ Teimpléad:CRC96
  49. ↑ 49.0 49.1 49.2 "Synthetic Studies in the Field of Fluorinated Cyclopropanes" (June 1956). Journal of the American Chemical Society 78 (12): 2801–2804. doi:10.1021/ja01593a041. 
  50. ↑ 50.0 50.1 "Vapor pressures, liquid molar volumes, vapor non-ideality, and critical properties of some partially fluorinated ethers (CF3OCF2CF2H, CF3OCF2H, and CF3OCH3), some perfluoroethers (CF3OCF2OCF3, c-CF2OCF2OCF2, and c-CF2CF2CF2O), and of CHF2Br and CF3CFHCF3" (as en) (October 1992). The Journal of Chemical Thermodynamics 24 (10): 1065–1075. doi:10.1016/S0021-9614(05)80017-5. 
  51. ↑ "The Preparation of Difluoroamino Sulfur Pentafluoride" (February 1963). Inorganic Chemistry 2 (1): 173–175. doi:10.1021/ic50005a044. 
  52. ↑ 52.0 52.1 52.2 52.3 52.4 "Substitution and Addition Reactions of the Fluoroölefins. IV. Reactions of Fluoride Ion with Fluoroölefins" (June 1960). Journal of the American Chemical Society 82 (12): 3091–3099. doi:10.1021/ja01497a028. 
  53. ↑ 53.0 53.1 "Preparation of N,N-difluoromethylamine and N,N-difluoroethylamine" (November 1960). Journal of Inorganic and Nuclear Chemistry 16 (1–2): 63–66. doi:10.1016/0022-1902(60)80088-7. 
  54. ↑ Advances in Inorganic Chemistry and Radiochemistry. - 1974. - Vol. 16. - p. 168
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  56. ↑ 56.0 56.1 Dictionary of organometallic compounds. - 2nd supplement. - Chapman and Hall Ltd, 1986. - p. 19
  57. ↑ "The Preparation and Properties of Trifluoromethoxy Sulfur Pentafluoride [CF3OSF5] and cis-Bis(trifluoromethoxy)tetrafluorosulfur(VI) [(CF3 O)2SF4 ]" (June 1964). Inorganic Chemistry 3 (6): 850–852. doi:10.1021/ic50016a015. 
  58. ↑ 58.0 58.1 "Perhaloalkyl hypochlorites and pentafluorosulfur hypochlorite. I. Preparation and properties" (March 1969). Journal of the American Chemical Society 91 (6): 1310–1313. doi:10.1021/ja01034a008. 
  59. ↑ 59.0 59.1 "(Trifluoroacetyl)sulfur pentafluoride" (September 1982). The Journal of Organic Chemistry 47 (19): 3772–3773. doi:10.1021/jo00140a039. 
  60. ↑ "New preparation for trifluoromethyl fluoroformyl peroxide and bis(trifluoromethyl) trioxide" (September 1970). Inorganic Chemistry 9 (9): 2182–2183. doi:10.1021/ic50091a045. 
  61. ↑ UNITED STATES PATENT 2,617,817 PERFLUOROALKYL ISOCYANATES Arthur H. Ahlbrecht, 11 November 1952
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  63. ↑ "363. The ethoxyfluorosilanes" (1949). J. Chem. Soc.: 1696–1699. doi:10.1039/JR9490001696. 
  64. ↑ 64.0 64.1 64.2 "Some perfluoroalkylsulfinyl halides. New preparations of trifluoromethylsulfur trifluoride" (September 1968). Journal of the American Chemical Society 90 (20): 5403–5408. doi:10.1021/ja01022a013. 
  65. ↑ 65.0 65.1 65.2 65.3 65.4 "Modern Inhalation Anesthetics" (as en) (1972): 418–439. Springer Berlin Heidelberg. doi:10.1007/978-3-642-65055-0_19. 
  66. ↑ 66.0 66.1 "Chemistry of Sulfur Tetrafluoride. III. Organoiminosulfur Difluorides" (February 1960). Journal of the American Chemical Society 82 (3): 551–555. doi:10.1021/ja01488a013. 
  67. ↑ "Perfluoro-1,2-dioxolane. A new synthesis and its gas-phase structure" (as en) (November 1992). Journal of Molecular Structure 274 (1): 163–170. doi:10.1016/0022-2860(92)80155-B. Bibcode: 1992JMoSt.274..163J. 
  68. ↑ "122. Some new ethyl and phenyl silicon fluorides" (1944). J. Chem. Soc.: 454–456. doi:10.1039/JR9440000454. 
  69. ↑ "Advances in Inorganic Chemistry and Radiochemistry" (as en) (1974). Academic Press. 
  70. ↑ "Trifluoromethyl thionitrite" (1969). Journal of the Chemical Society A: Inorganic, Physical, Theoretical: 1587. doi:10.1039/J19690001587. 
  71. ↑ 71.0 71.1 71.2 "Perfluoroalkyl Halides Prepared from Silver Perfluoro-fatty Acid Salts. II. Perfluoroalkyl Bromides and Chlorides" (March 1952). Journal of the American Chemical Society 74 (5): 1347–1350. doi:10.1021/ja01125a511. 
  72. ↑ 72.0 72.1 72.2 "Dictionary of Inorganic Compounds, Supplement 2" (as en) (1994). CRC Press. 
  73. ↑ "Pentafluoroguanidine" (May 1967). The Journal of Organic Chemistry 32 (5): 1662–1663. doi:10.1021/jo01280a103. 
  74. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."".
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  76. ↑ "Perfluoroalkyl chloroformates and chlorosulfates" (January 1969). Tetrahedron Letters 10 (9): 723–726. doi:10.1016/S0040-4039(01)87792-3. 
  77. ↑ "Modern Inhalation Anesthetics" (as en) (1972). Springer Berlin Heidelberg. doi:10.1007/978-3-642-65055-0_19. 
  78. ↑ 78.0 78.1 78.2 "Cóip cartlainne". Cartlannaíodh an bunleathanach ar Feabhra 15, 2017. Dáta rochtana: Iúil 17, 2022.
  79. ↑ Teimpléad:Cite thesis
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  81. ↑ "A New Synthesis of Bis-Trifluoromethyl-Phosphine, (CF3)2PH" (August 1957). Journal of the American Chemical Society 79 (15): 4242. doi:10.1021/ja01572a072. 
  82. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."".
  83. ↑ "Sulfur Pentafluoride Cyanate, F5S-O-C≡N" (February 1987). Angewandte Chemie International Edition in English 26 (2): 134–135. doi:10.1002/anie.198701341. 
  84. ↑ 84.0 84.1 84.2 "Structure and Stability of the Bromofluoroethylenes. II. The Geometric Isomers of 1-Bromo-1,2-difluoro- and 1,2-Dibromo-1,2-difluoroethylene" (July 1965). The Journal of Organic Chemistry 30 (7): 2121–2126. doi:10.1021/jo01018a002. 
  85. ↑ Anderson, H. H. (October 1962). "Boiling Points and Boiling Point Numbers of Organogermanium Compounds." (as en). Journal of Chemical & Engineering Data 7 (4): 565–567. doi:10.1021/je60015a041. ISSN 0021-9568. 
  86. ↑ "Advances in Organometallic Chemistry" (as en) (1964). Academic Press. 
  87. ↑ "A Trifluoromethylboron Compound, CF3BF2" (January 1961). Journal of the American Chemical Society 83 (1): 250–251. doi:10.1021/ja01462a053. 
  88. ↑ "Nitryl Cyanide, NCNO 2" (as en) (2014-07-01). Angewandte Chemie International Edition 53 (27): 6893–6897. doi:10.1002/anie.201404209. PMID 24861214. 
  89. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."".
  90. ↑ "Compounds of Germanium and Hydrogen. III. Monoalkylgermanes. IV. Potassium Germanyl. V. Electrolysis of Sodium Germanyl 1" (as en) (October 1950). Journal of the American Chemical Society 72 (10): 4706–4709. doi:10.1021/ja01166a100. ISSN 0002-7863. 
  91. ↑ "Addition of free radicals to unsaturated systems. Part VI. Free-radical addition to the nitroso-group" (1954). Journal of the Chemical Society (Resumed): 696. doi:10.1039/JR9540000696. 
  92. ↑ red brown gas
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  94. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."".
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  96. ↑ 96.0 96.1 "Nearest neighboring code and hydrogen bond index in labeled hydrogen-filled graph and graph of atomic orbitals: application to model of normal boiling points of haloalkanes" (December 2004). Journal of Molecular Structure: THEOCHEM 711 (1–3): 173–183. doi:10.1016/j.theochem.2004.10.003. 
  97. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."".
  98. ↑ Teimpléad:OrgSynth
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  101. ↑ "Experimental Study of Saturated Pressure Measurements for 2,3,3,3-Tetrafluoropropene (HFO-1234yf) and 2-Chloro-1,1,1,2-Tetrafluoropropane (HCFC-244bb)" (20 December 2013). Journal of Chemical & Engineering Data 59 (1): 157–160. doi:10.1021/je400970y. 
  102. ↑ "Fluorocarbon Derivatives. I. Derivatives of Sulfur Hexafluoride" (July 1957). Journal of the American Chemical Society 79 (13): 3424–3429. doi:10.1021/ja01570a029. 
  103. ↑ "Synthesis and properties of 2-(pentafluorothio)-3,3-difluorooxaziridine" (May 1980). Inorganic Chemistry 19 (5): 1330–1333. doi:10.1021/ic50207a045. 
  104. ↑ "Bis-monofluorcarbonyl-peroxyd" (7 March 1960). Angewandte Chemie 72 (5): 169. doi:10.1002/ange.19600720505. Bibcode: 1960AngCh..72..169A. 
  105. ↑ "Syntheses of Fluoroorganic Compounds" (as en) (2012). Springer Science & Business Media. 
  106. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."".
  107. ↑ "Some Perfluoroalkyliminosulfur Derivatives" (August 1966). Inorganic Chemistry 5 (8): 1317–1319. doi:10.1021/ic50042a004. 
  108. ↑ "Perhalodioxins and perhalodihydrodioxins" (June 1991). The Journal of Organic Chemistry 56 (12): 3915–3923. doi:10.1021/jo00012a026. 
  109. ↑ "394. Sulphur chloride pentafluoride: reaction with fluoro-olefins" (1961). Journal of the Chemical Society (Resumed): 2070. doi:10.1039/JR9610002070. 
  110. ↑ "Fluoroformic Acid Anhydride, FC(O)OC(O)F" (18 October 2002). Angewandte Chemie International Edition 41 (20): 3832–3834. doi:10.1002/1521-3773(20021018)41:20<3832::AID-ANIE3832>3.0.CO;2-M. PMID 12386862. 
  111. ↑ "Perfluorovinyl isocyanates" (November 1973). The Journal of Organic Chemistry 38 (22): 3924–3928. doi:10.1021/jo00962a022. 
  112. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."".
  113. ↑ "483. Organometallic and organometalloidal fluorine compounds. Part VIII. The electrochemical fluorination of dimethyl sulphide and carbon disulphide" (1953). J. Chem. Soc.: 2372–2375. doi:10.1039/JR9530002372. 
  114. ↑ "Trifluoromethyl trifluoromethanesulfonate (CF3SO2OCF3)" (January 1979). Tetrahedron Letters 20 (40): 3865–3866. doi:10.1016/S0040-4039(01)95545-5. 
  115. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."".
  116. ↑ "Inorganic Syntheses Volume 14" (as en) (2009). John Wiley & Sons. 
  117. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."".
  118. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."".
  119. ↑ "Partial fluorination of tetrahydrofuran with cobalt trifluoride" (as en) (1969). Journal of the Chemical Society C: Organic (13): 1739. doi:10.1039/j39690001739. ISSN 0022-4952. 
  120. ↑ "Ethoxyacetylene" (1954). Organic Syntheses 34: 48. doi:10.1002/0471264180.os034.15. 
  121. ↑ "584. Perfluoroalkyl derivatives of nitrogen. Part X. The reaction of nitric oxide with tetrafluoroethylene, and formation of a nitrosopolymer" (1962). Journal of the Chemical Society (Resumed): 3021. doi:10.1039/JR9620003021. 
  122. ↑ "Preparation and properties of germyl methyl ether and germylmethyl methyl ether" (as en) (November 1967). Inorganic Chemistry 6 (11): 1989–1994. doi:10.1021/ic50057a012. ISSN 0020-1669. 
  123. ↑ "One step synthesis of 1,1,1,4,4,4-hexafluorobutane from succinonitrile" (as en) (April 1999). Journal of Fluorine Chemistry 94 (2): 123–126. doi:10.1016/S0022-1139(98)00311-X. 
  124. ↑ "Phosphiran" (March 1967). Journal of the American Chemical Society 89 (5): 1102–1104. doi:10.1021/ja00981a013. 
  125. ↑ Earráid leis an lua: Invalid <ref> tag; no text was provided for refs named bu416
  126. ↑ Tá ort na shonrú' 'teideal = agus' 'url = nuair a úsáideann {{ lua idirlín}}."".
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