ライフサイエンスコーパス: dodecane

1 cluster compound (Au:SR, R = butane, hexane, dodecane).

2 c)(H), the acceptorless dehydrogenation of n-dodecane.

3 w that they do not cause mobilization of the dodecane.

4 r (RAFT) polymerization at 70 degrees C in n-dodecane.

5 multilamellar onions dispersed in deuterated dodecane.

6 re hepta- and octa-chlorinated undecanes and dodecanes.

7 icline, alpha-conotoxin MII, and bPiDDB (N,N-dodecane-1,12-diyl-bis-3-picolinium dibromide) blocked e

8 ating an unprecedented tricyclo[4.4.1.1(1,4)]dodecane-2,11-dione core.

9 series of less volatile C12-C16 n-alkanes (n-dodecane, 349 ppb; n-tridecane, 340 ppb; n-tetradecane,

10 (23) and 7-methyl-1,5,9-triazabicyclo[5.5.0]dodecane (39) do not enhance the stabilities of their mo

11 ms, while rearrangement to the bicyclo[7,3,0]dodecane (9-5) system leads to a mixture of olefin isome

12 beaded activated carbon (BAC) loaded with n-dodecane, a high molecular weight volatile organic compo

13 s, respectively) 2-6-fold in the presence of dodecane, a lipid-solubilizing agent, with 50% maximal a

14 This conclusion was supported by dodecane adsorption/desorption, which was independent of

15 ed during storage, while metabolites such as dodecane and 2,3-butanediol always decreased.

16 performed in three alkane solutions, decane, dodecane, and hexadecane.

17 ology is a definitive match of n-undecane, n-dodecane, and n-tridecane sample spectra to their corres

18 analogous experiments performed in anhydrous dodecane, and the observation that the silica "dissoluti

19 The catalytic C-H alumination of dodecane at 150 degrees C followed by quenching in air a

20 icationic 1,12-di(3-hexadecylbenzimidazolium)dodecane bis[(trifluoromethyl)sulfonyl]imide bromotrichl

21 (IL) monomer and 1,12-di(3-vinylimidazolium)dodecane bromide ([C(12)(Vim(+))(2)]2[Br(-)]) IL cross-l

22 ure helicene 3, either without solvent or in dodecane (but not in chloroform) aggregates into columna

23 ane (C(10)H(22)), undecane (C(11)H(24)), and dodecane (C(12)H(26)) at the tens of pmol level, release

24 r the first time for the photooxidation of n-dodecane (C12H26) in the presence of NOx in the CESAM ch

25 C-H alumination of dodecane catalyzed by 2 produces higher yields of the 1-

26 emperature (1)H NMR studies conducted in d26-dodecane confirm partial solvation of the PBzMA block at

27 (8)] 2[Br]) and 1,12-di (3-vinylimidazolium) dodecane dibromide ([(VIM)(2)C(12)] 2[Br]), were copolym

28 hain alkyl motifs were developed: a cysteine dodecane disulfide (Cdd) building block and a tyrosine-

29 ium in n-hexane (hex), n-octane (oct), and n-dodecane (dod).

30 forces transmitted across nanoscale films of dodecane down to a single molecular layer.

31 nsitive diazatetracyclo[4.4.0.1(3,10).1(5,8)]dodecanes (DTDs) with rare alicyclic scaffolding in high

32 iers for the stabilization of emulsions of n-dodecane emulsion droplets in water.

33 Ceramide in a dodecane/ethanol delivery system inhibited the opening o

34 The relatively low volatility of n-dodecane facilitates variable-temperature rheological st

35 mass organogelator (LMOG), in n-octane and n-dodecane have been investigated as their sols were trans

36 4-trimethylpentyl)dithiophosphinic acid in n-dodecane have been studied by visible absorption spectro

37 bic effect is examined from simulations of n-dodecane in different solvents.

38 sub-CMC concentrations on solubilization of dodecane in porous media under dynamic flow conditions.

39 ctane, n-nonane, n-decane, n-undecane, and n-dodecane) in blood using headspace solid-phase microextr

40 e as a third comonomer) also formed stable n-dodecane-in-water Pickering emulsions, as judged by opti

41 bb12 = bis[4(4'-methyl-2,2'-bipyridyl)]-1,12-dodecane), incorporated into a negatively charged model

42 on Modifier, when adsorbed at the iron oxide-dodecane interface at a shear rate of [Formula: see text

43 essfully used to characterise the iron oxide-dodecane interface at a shear rate of [Formula: see text

44 s containing the 12-oxatricyclo[6.3.1.0(2,7)]dodecane moiety having either the trans (8a-e) or cis (9

45 nt enhancements in activity (30.6 vs 3.6 mol(dodecane) mol(Pd)(-1) h(-1)) and selectivity (C(12):C(11

46 In this work a simulated collapse of an n-dodecane molecule in H2O, CCl4, and a water-like Lennard

47 -6-AO can be prepared with different oils (n-dodecane, n-decane, n-octane, soybean oil, olive oil, tr

48 size in six molecular solvents: n-hexane, n-dodecane, n-undecyl alcohol, chloroform, carbon tetrachl

49 )-octadien-2-one, (E)-2-nonenal, 2-decanone, dodecane, nonanoic acid, 2-(2-butoxyethoxy)ethyl acetate

50 a and log P in water versus both octanol and dodecane of 3 and a set of related agents.

51 d and 2-propanol, and one nonpolar molecule, dodecane, on LiNbO3(0001) was compared.

52 ophobic solvent components such as hexane or dodecane or by introducing hydrophobic electrolyte ions

53 altered after 1-h exposure to pure alkanes (dodecane or tetradecane) and alkane mixtures (mineral oi

54 arbamate (CNC) in an n-alkane (n-octane or n-dodecane) or 3beta-cholesteryl N-(2-naphthyl) carbamate

55 When bound to water droplets in dodecane, or to the plasma membranes of living cells, th

56 utadiene (PhBD) steric stabilizer block in n-dodecane produces either spheres or worms that exhibit l

57 noid featuring a novel tricyclo[4.4.1.1(1,4)]dodecane scaffold.

58 The membrane, impregnated with 2 M DOHA in dodecane, showed strong affinity for actinides and was s

59 The membrane, impregnated with 0.2 M DOHA in dodecane, showed very high selectivity for Pu(IV) in aci

60 By comparison, dodecane shows a preconcentration gain of approximately

61 o construct the unique tricyclo[6.3.1.0(1,5)]dodecane skeleton and the all-carbon quaternary center.

62 Two approaches to the aza-tricyclo dodecane skeleton of (-)-FR901483 are reported.

63 ts and kinetic gas-particle modeling for the dodecane SOA system, here we show that the presence of p

64 The results demonstrated the enhancement of dodecane solubility by monorhamnolipid surfactant at con

65 nel, about 15,000 plates were obtained for a dodecane test analyte.

66 e-human serum albumin clearing agent and 90Y-dodecane tetraacetic acid (DOTA)-biotin as the final ste

67 The NAPLs tested included dodecane, tetrachloroethylene, and jet fuel.

68 2,2,4-trimethylpentane (isooctane), decane, dodecane, tetradecane, hexadecane, and 2,6,10,14-tetrame

69 In the case of n-decane and n-dodecane, the resulting alkylarenes are exclusively unbr

70 d to be in the range of <1.0% per year for n-dodecane to n-hexadecane.

71 ting of representative components, including dodecane, toluene, and asphaltene).

72 are observed for a single molecular layer of dodecane trapped between crystallographically misaligned

73 mputer simulations of water, n-hexane, and n-dodecane under benchtop conditions shows that the sizes

74 roach to a dilute solution of Fe(CO)(5) in n-dodecane under VSC demonstrates polariton dephasing to t

75 ncentration with tributyl phosphate (TBP) in dodecane was the focus of this microscale study and was

76 air-water interface and less than 4% at the dodecane-water interface for bulk-water concentrations b

77 oil drop tensiometer at air/water (A/W) and dodecane/water (DD/W) interfaces.

78 re by 5%, the same as the surface tension of dodecane/water, in agreement again with the polymer brus

79 phobic interfaces [triolein/water (TO/W) and dodecane/water], were elastic, and were not pushed off t

80 levels of the alkanes decane, undecane, and dodecane were associated with sPTB in asymptomatic nulli

81 Decane, undecane, and dodecane were significantly associated with sPTB (FDR <

82 thylamino)propane and 1,8-diazabicyclo[6.3.1]dodecane, where ten and seven low-energy conformers, res