Index
A
A 3 (aldehyde-alkyne-amine) coupling, 266,
268
Acetophenone, 123
Acrolein, 349, 351, 352, 362, 363, 365, 377
Active phase dilution, 309, 334
A-cyclodextrin, 175–177
Ag, 111, 114, 115, 117, 118, 355, 362–366
Alcohol oxidation, 236, 237, 242
ALD cycles, 70, 75, 77, 78, 80–82, 84, 91
ALD process, 69–73, 75–80, 82–85, 90, 91,
93, 95, 97, 98
ALD reactor, 69, 71, 95, 97
Alkyl amines, 269
Allylic alcohol, 345, 348, 349, 360, 362, 366,
374, 378, 387, 389
Al 2 O 3 , 361–363, 372–374, 376, 390, 395,
409, 437, 438, 440
Al 2 O 3 ALD, 83, 84, 93
Amine ligands, 409, 410
Amino acid, 161, 162, 293
Aminopropyltriethoxysilane (APTS), 410
Aminopropyltrimethoxysilane, 354, 355
Aminothiolate ligand, 155
Andrussov reaction (cyanide synthesis, C–
N), 26
Aniline derivatives, 264, 269
Aryl amines, 265
Asymmetric hydrogenation, 420, 426, 429,
434–436
Atomic Layer Deposition (ALD), 69–72,
75–80, 82–84, 89–91, 93–97, 372,
374–376, 395
Au, 110, 117–119, 348–362, 365, 366, 369,
376, 381, 382, 385, 389, 390
Au NPs, 425
Azide-alkyne
cycloaddition
reaction
(CuAAC), 269
B
BASF process to menthol, 346
Benzalacetone, 349, 356, 357, 360, 361, 366,
367, 383, 389
Benzimidazolo[2,3-b]quinazolinones, 254
Benzodiazepines, 254
Benzofurans, 266, 268
Benzyl alcohol oxidation, 177, 181
Biaryl ketones, 260
Bimetallic, 310–314, 316, 317, 327
Bimetallic catalysts, 71, 72
Bimetallic core-shell, 71, 72, 79
Bis(diphenylphosphino)butane (dppb), 298,
417, 420, 437
Bmim, 380
BMIm (1-n-butyl-3-methylimidazolium),
114, 120
Bond cleavage energies, 298
Boride, 310, 315
Bottom-up syntheses, 251
Bromination of aromatics and alkynes (C–
Br), 21, 23
Buchner reaction, 17, 18
C
CAL, 347, 353, 354, 356–358, 360, 364,
367–383, 388–390, 393–397
Carbon–carbon bond–forming reactions, 15,
19
Carbon dioxide, 122, 124, 125
Carbon–heteroatom bond–forming reactions, 20
© Springer Nature Switzerland AG 2020
P. W. N. M. van Leeuwen and C. Claver (eds.), Recent Advances in Nanoparticle Catalysis,
Molecular Catalysis 1, https://doi.org/10.1007/978-3-030-45823-2
449
A
A 3 (aldehyde-alkyne-amine) coupling, 266,
268
Acetophenone, 123
Acrolein, 349, 351, 352, 362, 363, 365, 377
Active phase dilution, 309, 334
A-cyclodextrin, 175–177
Ag, 111, 114, 115, 117, 118, 355, 362–366
Alcohol oxidation, 236, 237, 242
ALD cycles, 70, 75, 77, 78, 80–82, 84, 91
ALD process, 69–73, 75–80, 82–85, 90, 91,
93, 95, 97, 98
ALD reactor, 69, 71, 95, 97
Alkyl amines, 269
Allylic alcohol, 345, 348, 349, 360, 362, 366,
374, 378, 387, 389
Al 2 O 3 , 361–363, 372–374, 376, 390, 395,
409, 437, 438, 440
Al 2 O 3 ALD, 83, 84, 93
Amine ligands, 409, 410
Amino acid, 161, 162, 293
Aminopropyltriethoxysilane (APTS), 410
Aminopropyltrimethoxysilane, 354, 355
Aminothiolate ligand, 155
Andrussov reaction (cyanide synthesis, C–
N), 26
Aniline derivatives, 264, 269
Aryl amines, 265
Asymmetric hydrogenation, 420, 426, 429,
434–436
Atomic Layer Deposition (ALD), 69–72,
75–80, 82–84, 89–91, 93–97, 372,
374–376, 395
Au, 110, 117–119, 348–362, 365, 366, 369,
376, 381, 382, 385, 389, 390
Au NPs, 425
Azide-alkyne
cycloaddition
reaction
(CuAAC), 269
B
BASF process to menthol, 346
Benzalacetone, 349, 356, 357, 360, 361, 366,
367, 383, 389
Benzimidazolo[2,3-b]quinazolinones, 254
Benzodiazepines, 254
Benzofurans, 266, 268
Benzyl alcohol oxidation, 177, 181
Biaryl ketones, 260
Bimetallic, 310–314, 316, 317, 327
Bimetallic catalysts, 71, 72
Bimetallic core-shell, 71, 72, 79
Bis(diphenylphosphino)butane (dppb), 298,
417, 420, 437
Bmim, 380
BMIm (1-n-butyl-3-methylimidazolium),
114, 120
Bond cleavage energies, 298
Boride, 310, 315
Bottom-up syntheses, 251
Bromination of aromatics and alkynes (C–
Br), 21, 23
Buchner reaction, 17, 18
C
CAL, 347, 353, 354, 356–358, 360, 364,
367–383, 388–390, 393–397
Carbon–carbon bond–forming reactions, 15,
19
Carbon dioxide, 122, 124, 125
Carbon–heteroatom bond–forming reactions, 20
© Springer Nature Switzerland AG 2020
P. W. N. M. van Leeuwen and C. Claver (eds.), Recent Advances in Nanoparticle Catalysis,
Molecular Catalysis 1, https://doi.org/10.1007/978-3-030-45823-2
449