ライフサイエンスコーパス: perfluoro

1 Electron transfer to perfluoro-1,3-dimethylcyclohexane in moist THF has yield

2 In this study, the PFAS alternative, perfluoro-1-butane-sulfonamide (FBSA), was identified fo

3 A new reagent, perfluoro-1-butanesulfonyl fluoride (PBSF), was used to

4 mpounds such as nonadecafluoro-1-decanol and perfluoro-1-octanol, while multiply charged oligonucleot

5 istinct PFC cores (perfluorooctylbromide and perfluoro-15-crown-5 ether).

6 magnetic resonance spectroscopy (MRS) and a perfluoro-15-crown-5-ether droplet in normal adult and n

7 tions of two rotamers in the hydrazone of 2H-perfluoro-2-methyl-3-pentanone can be altered from one e

8 Treatment of the hydrazone of 2H-perfluoro-2-methyl-3-pentanone with triethylamine at ele

9 omposition of the free-radical initiator bis(perfluoro-2-N-propoxyprionyl) peroxide (BPPP) was studie

10 The aromatic rings of perfluoro[2.2]paracyclophane are extremely reactive with

11 A synthesis of perfluoro[2.2]paracyclophane has been sought ever since

12 ons, including perfluorobutylethyl ether and perfluoro-2H-3-oxa-heptane, were performed employing UV,

13 nocations and perfluorotripentylamine and 2H-perfluoro-5,8,11-trimethyl-3,6,9,12-tetraoxapentadecane,

14 A series of oligothiophene-perfluoro-9-heterofluorene donor-acceptor (DA) compounds

15 ocol allows the introduction of a variety of perfluoro alkyl groups (C1-C10) and a CF2COOEt moiety.

16 (*-) to be considerably more stable than its perfluoro analogue.

17 aphthydrines (as well as their difluoro- and perfluoro-analogues) as a result of tandem direct cataly

18 The perfluoro- and perprotiopentaphenylboroles 1 and 2 react

19 ing 3570 possible compounds including C4-C10 perfluoro- and polyfluoroalkyl, polyfluorochloroalkyl ac

20 Functionalization of perfluoro aryl azides at various sites on BFCAs yields n

21 Functionalization of perfluoro aryl azides by bifunctional chelating agents (

22 lished in blood using time-of-flight MS with perfluoro coated Si-GLAD SALDI, by comparison to tabulat

23 goes thermal rearrangement to butadiene, the perfluoro compound will yield hexafluorocyclobutene upon

24 idene rearranges primarily to butadiene, its perfluoro counterpart is predicted to be an efficient pr

25 dicals C(n)H(2)(n)(-)(1) (n = 3-6) and their perfluoro counterparts C(n)F(2)(n)(-)(1) (n = 3-6).

26 complexes, and the calculations suggest that perfluoro dialkyl 10-X-2 ate-complexes should be experim

27 characterized by three halogen bond donors, perfluoro-iodophenyl groups.

28 onyl precursors [MCp(2)(CO)] each react with perfluoro-iso-propyl iodide without loss of CO, to affor

29 H(4))] reacts with perfluoro-n-butyl iodide, perfluoro-iso-propyl iodide, and pentafluorophenyl iodid

30 Mixtures of chloroform and perfluoro(methylcyclohexane) can be used as solvents for

31 n-solvent spin cross relaxation rates in the perfluoro(methylcyclohexane)-rich phase are considered.

32 acceptor, even surpassing the reactivity of perfluoro-n-alkyl iodides in that capacity.

33 lorate, chlorate, trifluoromethanesulfonate, perfluoro-n-butanesulfonate, perfluoro-n-octanesulfonate

34 (II) complex [MoCp(2)(C(2)H(4))] reacts with perfluoro-n-butyl iodide or perfluorobenzyl iodide with

35 ten precursor [WCp(2)(C(2)H(4))] reacts with perfluoro-n-butyl iodide, perfluoro-iso-propyl iodide, a

36 thanesulfonate, perfluoro-n-butanesulfonate, perfluoro-n-octanesulfonate, tetrafluoroborate, hexafluo

37 rboxylic acids (PFCAs; C6-15) along with six perfluoro-octane sulfonic acid (PFOS) precursors and 11

38 TFE and ammonium perfluoro-octanoate exposures were highly correlated, an

39 950-2002) was developed for TFE and ammonium perfluoro-octanoate, a chemical used in the polymerizati

40 Perfluoro-octanoate-PAGE analysis of detergent-solubiliz

41 of prestin by lithium dodecyl sulfate-PAGE, perfluoro-octanoate-PAGE, a membrane-based yeast two-hyb

42 Chemical cross-linking experiments, perfluoro-octanoate-PAGE/Western blot, and affinity puri

43 f human ABCG2 using non-denaturing detergent perfluoro-octanoic acid and Triton X-100 in combination

44 ow that PagP, initially unfolded in 5% (w/v) perfluoro-octanoic acid or 6 M guanidinium chloride, ins

45 cells, we analyzed oligomer formation using perfluoro-octanoic acid polyacrylamide gel electrophores

46 us endocrine disrupting chemicals including, perfluoro-octanoic acid, tributyltin, and butylhydroxyto

47 Trimeric perfluoro-ortho-phenylene mercury (1) crystallizes from

48 When performed on a mesoporous Si wafer, the perfluoro reagent yields a superhydrophobic surface (con

49 We focus in particular on hydrated perfluoro-sulfonic acid compounds employed as electrolyt

50 anol (TFE), hexafluoropropan-2-ol (HFP), and perfluoro-tert-butanol (PFTB).

51 each synthesis was a Mitsunobu reaction with perfluoro-tert-butanol, which incorporated a perfluoro-t

52 yclopentane (16) or pentane (17-19); OR(f) = perfluoro-tert-butoxy) via photolysis of the precursor c

53 nct conformational preferences, with (2S,4R)-perfluoro-tert-butyl 4-hydroxyproline promoting polyprol

54 (2S,4R)- and (2S,4S)-perfluoro-tert-butyl 4-hydroxyproline were synthesized (

55 di-tert-butylbenzene in solvents composed of perfluoro-tert-butyl alcohol, tetramethylsilane, and car

56 tractive interactions between the solute and perfluoro-tert-butyl alcohol.

57 lear NMR ((19)F:fluoro; pentafluorophenyl or perfluoro-tert-butyl ether; 4,4-difluoro; (77)SePh) and

58 perfluoro-tert-butanol, which incorporated a perfluoro-tert-butyl group, with nine chemically equival

59 lene analogues [MCp(2)(C(2)H(4))] react with perfluoro-tert-butyl iodide to yield the products MCp(2)

60 ide-based pharmaceuticals, a novel geminally perfluoro-tert-butylated beta-amino acid (betaFa) and it

61 Cesium bis(perfluoro-triphenylborane)amide, Cs[H2NB2(C6F5)6] (1), h