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You can also use the keyboard to select a range. Navigate to the first cell in the range. Press and hold while using an or , to arrow key, such as select the remaining cells in the range.

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Use free spire.doc library you can simply convert word to pdf without Word: //Load Document. Document document = new Document(); document.LoadFromFile(@"E:\work\documents\TestSample.docx"); //Convert Word to PDF. document.SaveToFile("toPDF.PDF", FileFormat.PDF);

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31 Oct 2018 ... Steps to convert word document to PDF programmatically: Create a new C# console application project. Install the Syncfusion.DocToPDFConverter.WinForms NuGet packages as reference to your . NET Framework application from NuGet.org. Include the following namespaces in the Program.cs file.

Fig. 3-22 Dependence of number-average molecular weight (*) and polydispersity index (4) on monomer conversion for ATRP polymerization of bulk styrene at 110 C with CuBr, 1-phenylethyl bromide (I), and 4,4-di-5-nonyl-2,20 -bipyridine (L). M 0:087 M; CuBr 0 L 0 =2 I 0:087 M. After Matyjaszewski et al. [1997] (by permission of American Chemical Society, Washington, DC); an original plot, from which this gure was drawn, was kindly supplied by Dr. K. Matyjaszewski.

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Is there any free .net library to convert word to pdf in asp.net, c# application. ... converting-word-doc-file-to-pdf-without-using-microsoftofficeinteropwor.aspx .... LoadFromFile(@"E:\work\documents\TestSample.docx"); //Convert ...

Equation 3-227 shows that for any except a very-low-molecular-weight polymer, the size distribution will be very narrow with (X w =X n ) being close to unity. For a polymer of numberaverage degree of polymerization of 50 having a Poisson distribution, the PDI would be 1.02. For the ATRP polymerization in Figure 3-22, PDI is about 1.05, very close to the theoretical value. Many ATRP polymerizations have somewhat broader distributions (PDI 1.2 1.3) for two reasons. First, there is the very initial period (as much as 5% conversion) before the persistent radical (deactivator) concentration has grown suf ciently large to suppress normal termination. Most of this problem can be avoided by initially adding CuBr2 ($10 mol% of CuBr). Second, at very high conversion ($90%), the polymerization rate decreases significantly such that normal termination is not suf ciently suppressed. For the successful synthesis of block copolymers, the second monomer should be added no later than $90 95% conversion, not at 100% conversion. 3-15b-2 Effects of Components of Reaction System

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A variety of monomers, including styrene, acrylonitrile, (meth) acrylates, (meth) acrylamides, 1,3-dienes, and 4-vinylpyridine, undergo ATRP ATRP involves a multicomponent system of initiator, an activator catalyst (a transition metal in its lower oxidation state), a deactivator (the transition state metal in its higher oxidation state) either formed spontaneously or deliberately added, ligands, and solvent Successful ATRP of a speci c monomer requires matching the various components so that the dormant species concentration exceeds the propagating radical concentration by a factor of $106 Various organic halides are used, including alkyl halides such as CHCl3 and CCl4 , allyl and benzyl halides, a-haloesters, a-haloketones, a-halonitriles, and sulfonyl halides Fast and quantitative initiation is needed to achieve narrow molecular weight distributions, but an initiator that decomposes too rapidly results in increased normal bimolecular termination of propagating radicals.

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Bromides are more reactive than chlorides, iodides are highly reactive but undergo light-induced side reactions, and uorides are unreactive The initiator reactivity should be matched to the monomer reactivity In general, this is achieved by using a halide with an organic group similiar in structure to the propagating radical, for example, benzyl halide, a-haloester, and a-halonitrile for styrene, acrylate, and acrylonitrile polymerizations, respectively The metal catalyst must have two oxidation states easily accessed by a one electron transfer, an af nity for halogen, an expandable coordination sphere to accomodate the halogen, and a strong complexation with the ligand The catalyst is the key to ATRP since it determines the position of equilibrium (value of K) and rate of exchange between dormant and propagating species Various middle and late transition metals (groups 6 11) have been investigated.

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Catalysts based on copper are the most studied and have found the greatest utility, as they are useful irrespective of the monomer Proper functioning of a metal catalyst requires appropriate ligands Ligands solubilize the transition metal salt in organic media and adjust the redox potential of the metal center for appropriate activity For copper catalysts, bidentate and multidentate, but not monodentate, nitrogen ligands work best Bridged and cyclic ligands as well as branched aliphatic polyamines yield more active catalysts than do simple linear ligands 4,4-Dialkyl-2,20 -bipyridines and tris-(2-dimethylaminoethyl)amine.

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