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The porphyrin handbook - Kadish K.M.

Kadish K.M. The porphyrin handbook - Academic press, 2000. - 368 p.
Download (direct link): kadishsmishgulilard2000.djvu
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Polymeric metalloporphyrins, 232 Polymeric porphyrins, conductive See
Porphyrin polymers, conductive Polymerization, See Addition
polymerization; Controlled polymerization; Ring-opening polymerization
Poly(methyl methacrylate), synthesis, 145 Porous porphyrin structures,
73-74, 77 Porphocyanine, structural formula, 211 Porphycenes, 196-198
Porphyrin aggregates, See Multiporphyrin assemblies, noncovalent
Porphyrin arrays, 67, 69-72, 75, 77, 78, 87 vapor detector, 119-120, 123
Porphyrin-based chemical sensors, 114-127 Porphyrin-based electrochemical
sensors,
231-255 Porphyrin-based membranes, 122 Porphyri n-based
photosensitizers, 161 -164 Porphyrin-bridged donor-acceptor molecules,
55, 56
Porphyrm-calixarene, 310-311 Porphyrin-cyclocholate molecular bowl, 125,
126
Porphyrin-cyclodextrin, 310-311 Porphyrin dimers, See Dimeric porphyrins
Porphyrinic solids, 72
chemical sensors, 114-127 conductive polymers, 102-103, 105, 107,
109, III
ferroelectrics, 111-113, 117, 118 microporous solids, 72-74, 77-102
Porphyrin-incorporated zeolites, 87-88, 90-91,93,94, 112, 113
Porphyrinoids, 207 dimerization, 8 Porphyrin-oligothiophene polymers,
synthesis, 117
Porphyrin polyimide, 56, 58, 59 Porphyrin polymers, conductive, 102-103,
105
covalent conjugated porphyrin polymers,
107, 109, 115, 116 linked polymers and arrays, 111
"shish kebab polymers," 105, 107, 114 Porphyrin-quinone assembly, 320
Porphyrin-quinone complexes
as artificial photosynthesis system, 63-65 as photodonor, 317
Porphyrins
from ALA, 208-209 association and dissociation rates, 311 barbituric
acid functionalized, 206, 217 basket handle porphyrins, 60 boronic-acid-
appended, 281, 283, 303 cationic, 209-211, 221, 222 chemically modified,
280-281 chiral, 285-287 conformational dynamics, 311 covalently linked,
326-328 cyclodextrin-appended, 317 cytochrome binding porphyrins, 322-
323 dendrimer-porphyrins, 126 dimers. See Dimeric porphyrins double-
decker porphyrins, 287 expanded, 204-205, 211 glycosylated, 205-206, 213-
216 host-guest chemistry, 280, 287-312 hydroquinone-appended, 316
Index
345
intercalation on clays, 94-95, 98 inverted, 198, 199 isomeric. 196-198
in layered double hydroxides (LDH), 44, 101-102, 113, 114 mesogenic,
44-53 metal-bridged porphyrin dimer, 30 molecular boxes, 30
multiporphyrin assemblies, noncovalent, 1-41
naturally occurring, 280-281 ".V-confused." 198
as nonlinear optical (NLO) materials, 44,
53-62
nucleoside adducts. 206, 218 oligoporphyrins, 284-285 optical limiting
properties, 61-62 as opto-materials. 65- 72 phosphorescence, quenching. I
14-1 15 as photosensitizers m PDT. 161-225 picket-fence porphyrins, 164.
282 "picnic basket" porphyrins. 121 polymeric. 232-236 porphynn-
calixarene, 3 10-3 1 I porphyrin-cvelodextrin, 310-31 I porphyrin-
steroids. 3 10-3 11 properties. 44. 232. 280 "push-pull" porphyrins. 54-
56 as receptor molecules, 28 I -336 as receptors for alcohol recognition.
300-303
as receptors for amine recognition,
287-245
as receptors for amino-acid derivative recognition. 297-300 as
receptors for amino-acid recognition,
291-297
as receptors foi diamine recognition, 287-292 as receptors for DNA
recognition,
304-306, 308 as receptors for quinone recognition. 303-304
as receptors for sugar recognition, 300-303 self-assembling, 328-336
"ship-in-bottle" porphyrin system. 90-91, 94 with six-membered rings,
207. 218, 219 solids. Sec Porphyrinic solids solubility of, 283
strapped porphyrins. 52. 284. 285. 287 tautomerism, 20. 2 I triangular
porphyrin aggregate, 30 two-point coordination of, 22-23 uses in material
chemistry, 44 v inylogous porphyrins, 205, 2 I 3 Porphyrin sponges, 73-
74, 77. 79-82 Porphyrin-steroids. 310-311 Potentiometric porphyrinic
sensors ion detection, 251-255 for nickel. 254-255 Prerotaxane. 38, 39
Protoheme. 281. 283
chemically modified, 281 Protoporphyrin IX, 280-281 Protoporphyrin IX
analogues. 162. 162-163 Purpurin 18, 164
chemical modification of, 167-172 Purpurin-1 8 N-alkvliimdes,
formation of. 166 Purpurin isoimides, formation of, 167-168
Purpurins
as photosynthesizers, 174, 178 preparation of, 177 "Push-pull"
porphyrins, 54-56 5-(4-Pyridyl (porphyrin, 23 Pyriporphyrinone, 207
Pyropheophorbides, 164-165
Q
Quaternary ammonium metalloporphyrins, 124 Quinone-cyclophane-porphyrin
triad. ,320 Quinone recognition, porphyrin-based receptors, 303-304
R
Reaction centers (RC), 2-3, 9-10 Receptor molecules, 281-284 alcohol
recognition. 300-303 amine recognition, 287-295 amino-acid derivatives
recognition.
297-300 amino-acid recognition, 291-297 chiral porphyrins. 285-
287 diamine recognition, 287-292 DNA recognition, 305-306. 308
multifunctional porphyrins as building blocks, 28 1-284 naturally
occurring porphyrins, 280-281 oligoporphyrins, 284-285 porphynn-
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