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Anhydrous dichloromethane dcm

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Anhydrous dichloromethane (DCM) is a colorless, volatile liquid commonly used as a solvent in various laboratory applications. It has a molecular formula of CH2Cl2 and a molar mass of 84.93 g/mol. Anhydrous DCM is characterized by its high purity, with low levels of water content, making it suitable for sensitive chemical reactions and analyses where the presence of water could interfere with the process.

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6 protocols using anhydrous dichloromethane dcm

1

Synthesis of Organic Compounds Using Common Reagents

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Anhydrous dichloromethane (DCM) and tetrahydrofuran (THF) were purchased from Sigma Aldrich. Absolute ethanol was obtained from Decon Laboratories. Diethyl ether (Et2O), methyl tert‐butyl ether (MTBE), and sodium azide were purchased from Fisher Scientific. Triethylamine (NEt3) and methanesulfonyl chloride (MsCl) were obtained from Acros and distilled from CaH2 and P2O5, respectively. Trifluoroacetic acid (TFA) was purchased from Oakwood Products. Pearlman's catalyst (Pd(OH)2/C), 2,2,6,6‐tetramethylpiperidine‐1‐oxyl (TEMPO), phenylacetylene (PA), diphenylacetylene (DPA), dimethyl acetylenedicarboxylate (DMAD), and diethyl acetylenedicarboxylate (DEBD) were purchased from Sigma Aldrich and used as received. Potassium bromide and di‐tert‐butyl dicarbonate ((Boc)2O) were purchased from Acros and used as received.
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2

Synthesis and Characterization of Phthalocyanine Compounds

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Copper (II) phthalocyaninetetrasulfonic acid (CuPcS4) tetrasodium salt, tetrabutylammonium (TBA) bromide, tetrabutylphosphonium (P4444) bromide, 3-(dodecyldimethyl-ammonio)propanesulfonate (DDMA), anhydrous methanol, anhydrous 1-propanol, anhydrous dichloromethane (DCM), anhydrous chloroform, anhydrous toluene, anhydrous heptane, hexane, and anhydrous benzene were purchased from Sigma-Aldrich (St. Louis, MO USA). Tributyl-n-octylphosphonium (P4448) bromide was purchased from TCI (Portland, OR USA). Xylenes was purchased from Mallinckrodt (Paris, KY USA) and ethanol was purchased from Koptec (King of Prussia, PA USA). All chemicals were used as received without further purification.
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3

Functionalization of DC Bead Microspheres

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DC Bead® intermediate (Acrylamido Polyvinyl Alcohol-co-Acrylamido-2-methylpropane sulfonate microspheres, dried to a free-flowing powder and untainted) was obtained from Biocompatibles UK Ltd, a BTG International group company, Camberley, UK. Anhydrous dimethyl sulfoxide (DMSO), 1,1′-Carbonyldiimidazol (CDI), 2,3,5-Triiodobenzyl alcohol, 2,3,5-Triiodobenzoic acid, N,N′-Diisopropylcarbodiimide (DIC), 1-Hydroxybenzotriazole hydrate (HOBt), 4-(Dimethylamino)pyridine (DMAP), Trimethylenediamine, Triethylamine (Et3N), and anhydrous Dichloromethane (DCM) were purchased from Sigma Aldrich (Milwaukee, WI). Doxorubicin (Dox) was obtained from Bedford Laboratories® (Bedford, OH). De-ionized water (DI water) was obtained from in house filtration system (Hydro Inc. Rockville, MD).
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4

Synthesis and Characterization of DSPE-PEG Nanoparticles

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Distearoylphosphatidylethanolamine–polyethylene glycol (DSPE–PEG, PEG Mw of 550 and 2000 Da) were purchased from Avanti polar lipids (Alabama, USA). Distearoylphosphatidylethanolamine (DSPE) and hydrogenated soy phosphatidylcholine (HSPC) were purchased from Lipoid (Ludwigshafen, Germany). Triethylamine (99%), 2-(methacryloyloxy)ethyl phosphorylcholine (MPC), copper(i) bromide (CuBr, 99.999%), 2-bromoisobutyryl bromide (BIBB, 98%), N,N,N,N′′,N′′-pentamethyldiethylenetriamine (PMDETA, 99%), bovine serum albumin (BSA), anhydrous dichloromethane (DCM), and anhydrous chloroform were purchased from Sigma-Aldrich (Israel). DiR (1,1′-dioctadecyl-3,3,3′,3′-tetramethylindotricarbocyanine iodide), DiI (1,1′-Dioctadecyl-3,3,3′,3′-tetramethylindocarbocyanine perchlorate), fetal bovine serum (FBS), and RPMI-1640 medium were purchased from Thermo Fisher Scientific (UK). Hyaluronate-DyLight 755 (2.5 MDa) was purchased from Creative PEG Works (US).
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5

Synthesis of Fluorescent Imaging Probes

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Camptothecin (CPT), IR-820, 2-hydroxyethyl disulfide (HEDS), 1, 6-hexanediol, triphosgene, 4-nitrophenyl chloroformate, 4-dimethylaminopyridine (DMAP), and other reagents were purchased from Sigma-Aldrich (USA). The solvents anhydrous dimethylformamide (DMF), and anhydrous dichloromethane (DCM) were also acquired from Sigma-Aldrich (USA). Fetal bovine serum (FBS) and Dulbecco’s modified Eagle’s medium (DMEM) were purchased from Gibco. All other reagents and solvents were of analytical or chromatographic grade.
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6

Synthesis and Characterization of Functionalized Nanoparticles

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The following materials were used as received: methoxy polyethylene glycol 1000 Da (PEG1000) (Sigma-Aldrich), triethylamine (TEA) (99.5%, Sigma-Aldrich), pyridine (99.8%, Sigma-Aldrich) p-nitrophenyl chloroformate (pNPCF) (98%, Sigma-Aldrich), 2,5-dihydroxybenzoic acid (2,5-DHB) (Sigma-Aldrich), anhydrous dichloromethane (DCM) (Sigma-Aldrich), dimethyl sulfoxide (DMSO) (Acros Geel), K2PtCl4 (min. 42.4% Pt, Alfa Aesar), n-octanethiol (C8) (98%, Sigma-Aldrich), deuterium oxide (D, 99.96%, Cambridge Isotope Laboratories), and phosphate buffer (10x, Lief Technologies). Fourth generation amine terminated PAMAM dendrimers were purchased as 10% by weight solutions in methanol (Sigma-Aldrich, St. Louis, MO). Silica gel 60 A 230–400 mesh ATSM (Whatman Inc) and silica gel 60 F254 plastic sheets (TLC) (Merck KGaA) were used for column and thin layer chromatography, respectively. Ultrapure water (≥18 MΩ·cm, Millipore Milli-Q) and 200 proof ethanol (Gold Shield Chemical Co.) were used for dilution and washing. Ultrapure N2 (98%, Air Gas Co.) and H2 (99.99%, Praxair, Inc.) were used for drying and flaming, respectively. Tungsten wire (d = 0.010 in., 99.95%, California Fine Wire Co.) was used to make STM tips. Au slugs (99.99%, Alpha Aesar Premion Co.) and mica (clear ruby muscovite, Mica New York Corp.) were used for Au thin film preparation.
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