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101 protocols using octadecene

1

CsPbBr3 Nanocrystal Synthesis

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The CsPbBr3 NCs were prepared by using the hot injection technique previously described in the literature.[57] Briefly, for the Cs‐oleate preparation, Cs2CO3 (0.0814 g, Aldrich, 99.9%) was loaded into 10 mL 3‐neck flask with octadecene (10 mL, Sigma‐Aldrich, 90%) and oleic acid (1 mL, OA, Sigma‐Aldrich, 90%), stirred for 10 min at room temperature, and then heated under N2 to 150 °C before injection. Simultaneously, 0.414 g PbBr2 was loaded into 25 mL 3‐neck flask and then octadecene (30 mL, Sigma‐Aldrich, 90%), oleylamine (3 mL, OLA, Sigma‐Aldrich, 90%), and OA (3 mL, OLA, Sigma‐Aldrich, 90%) were injected. After stirring, the system was heated to 180 °C under N2. Cs‐oleate solution (3 mL, prepared as described above) was quickly injected and, 5 s later, the reaction mixture was cooled by the ice‐water bath. After filtering and purification, the 5 mg mL−1 methylbenzene‐based CsPbBr3 nanocrystal solution was prepared for use.
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2

Synthesis of PbS Colloidal Quantum Dots

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PbS colloidal quantum dots (CQD) were
synthesized according to previously published methods. First, 460
mg of lead(II) oxide (PbO, 99.999%, Sigma-Aldrich) was mixed with
10 mL of octadecene (technical grade, Sigma-Aldrich) and 2 mL of oleic
acid (technical grade, Sigma-Aldrich). The solution was heated to
120 °C and degassed for 1 h. Then the temperature was reduced
to 90 °C and 5 mL of octadecene solution with 140 μL of
hexamethyldisilathiane (TMS2S) (synthesis grade,
Sigma-Aldrich) was injected swiftly. After the injection, heating
was turned off and the solution was allowed to cool to room temperature
gradually. The as-synthesized CQD-solution was purified by adding
acetone (VWR) before centrifugation at 6000 rpm for 5 min, followed
by redispersing with hexane (95%, Sigma-Aldrich). This washing process
was repeated twice, and the precipitate was dispersed by octane (50
mg/mL).
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3

Synthesis of Colloidal Nanocrystals

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Copper(II) chloride [CuCl2, 97%], cobalt(II) chloride [CoCl2, 97%], octadecene [ODE,
90%, technical grade], and di-tert-butyl disulfide
[DTBDS, 97%] were purchased from Sigma-Aldrich. Zinc chloride [ZnCl2, 99.95%] and cadmium chloride [CdCl2, 99.99%]
were purchased from Alfa Aesar. Benzyl ether [BE, 99%] was purchased
from Acros Organics. Trioctylphosphine [TOP, >85%] was purchased
from
TCI America. All solvents (hexanes, isopropyl alcohol [IPA], acetone,
and toluene) were of analytical grade. All of the above chemicals
were used as received without further purification. Distilled oleylamine
[d-OLAM] was obtained via vacuum
distillation of oleylamine [t-OLAM, 70%, technical
grade, Sigma-Aldrich].24 (link)
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4

Synthesis of Silver Nanoparticles

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Octadecene (95%, Sigma-Aldrich),
OAm (Loba), benzyl alcohol (99% Sigma-Aldrich), silver(I) nitrate
(AgNO3) (99%, Sigma-Aldrich), ethanol (EtOH) (spectroscopy
grade), and chloroform (high-performance liquid chromatography grade)
were used.
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5

Synthesis of CsPbBr3 Quantum Dots

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The synthesis of CsPbBr3 QDs is according to the previously reported hot-injection method with minor modifications25 (link). Octadecene (4 ml, Sigma-Aldrich, 90%) and PbBr2 (69 mg, Aladdin, 99.999%) were mixed in a 50 ml four-neck flask and dried under N2 for 50 min at 120 °C. Then, oleylamine (1 ml, Aladdin, 80–90%) and oleic acid (0.5 ml, Aladdin, >90%) were injected into the flask; after 20 min at 120 °C under N2, the temperature was raised to 170–190 °C (for tuning the nanocrystals size), hot Cs-oleate (0.4 ml, 0.1 M in ODE, prepared above) was rapidly injected, and 5 s later, the reaction mixture was cooled in the ice-water bath. The resulting NCs were dispersed into toluene for self-assembly.
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6

Synthesis of Rare-Earth Nanocrystals

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The nanocrystals were synthesized by thermal decomposition method in boiling oleic acid and octadecene acting as solvents51 (link),61 (link).
Neodymium(III) acetate hydrate ((CH3CO2)3Nd·3H2O with 99.9% purity), yttrium(III) acetate hydrate ((CH3CO2)3Y·3H2O with 99.9% purity), gadolinium(III) acetate hydrate ((CH3CO2)3Gd·3H2O with 99.9% purity), ammonium fluoride (NH4F of 98% purity), acetic acid (CH3CO2H of 99% purity), oleic acid (CH3(CH2)7CH=CH(CH2)7COOH of 90% purity) and 1-octadecene (CH3(CH2)15CH=CH2 with 90% purity) were purchased from Sigma Aldrich. Sodium hydroxide (NaOH with 99.8% purity), ethanol (C2H5OH, 96% pure p.a.), methanol (CH3OH, 99.8%), n-hexane (C6H14, pure p.a.) and chloroform (CHCl3, 98.5%) were purchased from POCH S.A. (Poland). Lithium hydroxide (LiOH anhydrous with 99% purity) were purchased from Pol-Aura. All of the chemical reagents were used as received without future purification.
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7

Synthesis of Copper-based Nanomaterials

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Copper (I) chloride (99.99%, STREM), Oleylamine (Oam, 95%, STREM), Oleic acid (OA, 90%, Aldrich), Octadecene (ODE, 90%, Sigma-Aldrich), Copper (I) acetate (ABCR), Copper (II) acetylacetonate (97%, Sigma-Aldrich), TOPO (Strem, 99%), chlorobenzene (anhydrous, 99.8%, Sigma-Aldrich), Sulfur (99.998%, Sigma-Aldrich), 1-dodecanethiol (98%, Sigma Aldrich), Toluene (99.9%, Sigma-Aldrich), Ethanol (Fluka), Hydrazine (Gerling Holz+Co), Acetonitrile (ACN, max. 0.005% H2O, Merck), Copper (II) sulfide (CuS, 99.5%, STREM), Copper (I) sulfide (Cu2S, 99.5%, Alfa Aesar), Magnesium-bis(hexamethyldisilazide (Mg(HMDS)2, 97%, Sigma-Aldrich), Magnesium bis(trifluoromethanesulfonyl)imide (Mg(TFSI)2, 99.5%, Solvionic), Magnesium chloride (MgCl2, 99.9%, Alfa Aesar), Tetraglyme (99%, ABCR).
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8

Fluorescent Probe Synthesis and Characterization

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Chlorotrimethylsilane, tetramethylammonium hydroxide pentahydrate (TMAH), cadmium oxide (CdO), octadecene (ODE), zinc oxide (ZnO), trioctylphosphine oxide (TOPO), selenium (Se), (3-aminopropyl)trimethoxysilane (3-APTMS), trioctylphosphine (TOP), hexadecylamine (HDA), sulfur, succinic anhydride, rhodamine 6G, N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDC), N-hydroxysuccinimide (NHS), HAuCl4·3H2O, tannic acid, TGA, MPA, l-cysteine, and GSH were purchased from Sigma Aldrich Co. LLC. (Saint Louis, MO, USA). Oleic acid was purchased from Nacalai Tesque Inc. (Kyoto, Japan). Methanol, tri-sodium citrate and potassium hydroxide (KOH), methanol, acetone, and chloroform were purchased from Wako Pure Chemical Ind. Ltd. (Osaka, Japan). An ultrapure Milli-Q Water System was used for sample preparation. The MB and synthetic DNA targets were purchased from FASMAC Co. Ltd. (Atsugi, Kanagawa, Japan). Black hole quencher-2 (BHQ-2) was used as the fluorescence quencher.
MB sequence: 5′-/NH2/GCGACTTTCAGTTATTATGCCGTTGTATTTGTCGC/BHQ-2/-3′
Full complementary DNA: AAATACAACGGCATAATAACTGAAA
Single nucleotide DNA: AAATACAACGTCATAATAACTGAAA
Noncomplementary DNA: TGAAGCTAACCGGTAAGCGCTATAG
The bold sequence is the stem sequence of the MB.
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9

Synthesis of Colloidal Semiconductor Nanocrystals

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Cadmium oxide (CdO, 99.99%), oleic acid (90%), tri-n-octylphosphine (TOP, 90%), trioctylphosphine oxide (TOPO, 99%), octadecene (ODE, 90%), selenium (Se, 99.999%), sulfur (S, 99.5%), 1,4-benzenedithiol (1,4-BDT, 99%), diethylene glycol (DEG, 99%), oleic acid (OA, 90%) and all organic solvents were purchased from Sigma-Aldrich and used without further purification. Octadecylphosphonic acid (ODPA) was purchased from PCI Synthesis. Thiophenol (TP, 98%) was purchased from Merck.
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10

Synthesis of Fatty Acid Acetate

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FA acetate (3.765 mmol, 0.392 g, Aldrich, 99%) was loaded into a 50 mL three-neck flask along with octadecene (ODE, 18 mL) and oleic acid (12 mL, Sigma-Aldrich, 90%). The reaction mixture was degassed three times at room temperature, heated to 100 °C under nitrogen until the reaction was completed and cooled down to room temperature. The obtained solution was stored in a glovebox.
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