戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (left1)

通し番号をクリックするとPubMedの該当ページを表示します
1                                              ROMP of N-trimethylsilyl norbornenes rendered the prepar
2                                              ROMP reactions could be stopped using MIM (1-5 equiv) an
3                                              ROMP reactions in neat COE and NBD could be inhibited fo
4 rdinated complexes in representative RCM and ROMP reactions.
5 s as alternatives to traditional metal-based ROMP initiators to allow the preparation of polymers wit
6  (ROMP) reactions of cyclooctene (COE), bulk-ROMP reactions of COE and norbornadiene (NBD), and ring
7 c approach and the length control offered by ROMP, we assemble block copolymers capable of traversing
8 repare pure, high MW bottlebrush polymers by ROMP grafting-through.
9  variety of polymers that may be prepared by ROMP and be of general use with norbornyl oligopeptides
10 density oligopeptide polymers synthesized by ROMP is dramatically improved upon addition of LiCl to r
11 ning triazolylbiferrocene are synthesized by ROMP or radical chain reactions and react with HAuCl4 to
12 s-ring-opening metathesis polymerization (CM-ROMP) strategy that affords functionalized Grubbs-II ini
13 e of endo-dicyclopentadiene (DCPD), a common ROMP monomer, to form linear polyDCPD and copolymers wit
14 s the first metal-free method for controlled ROMP.
15  3 was successfully demonstrated in a couple-ROMP-filter protocol utilizing in situ polymerization, a
16 monomers that can be utilized for metal-free ROMP.
17                     The hydrogenated ROMP (H-ROMP) resin was found to be highly resistant to acidic,
18 similar results were obtained for both the H-ROMP and PS-DVB resins.
19                                        The H-ROMP resin was found to have superior performance compar
20                             The hydrogenated ROMP (H-ROMP) resin was found to be highly resistant to
21 ere isolated, characterized, and employed in ROMP and RCM experiments where they exhibited very low c
22                       In the first instance, ROMP of 5-acetyloxycyclooct-1-ene (ACOE) followed by eff
23  development of a rate law describing living ROMP initiated by a Grubbs third-generation catalyst tha
24 se traditionally obtained via metal-mediated ROMP.
25 ndergo ring-opening metathesis (ROM) but not ROMP.
26                             Because numerous ROMP and NCA monomers are widely available, this novel p
27  polymerizable norbornene-on the kinetics of ROMP of polystyrene and poly(lactic acid) MMs initiated
28                                           PA-ROMP is a unique polymerization method that employs a sy
29                             Additionally, PA-ROMP was used to prepare nearly perfect block copolymers
30 is-4-octene as a CTA, the capabilities of PA-ROMP were investigated with a Symyx robotic system, whic
31 n ring-opening metathesis polymerization (PA-ROMP).
32 ed to design several experiments in which PA-ROMP was performed from one to ten cycles.
33  ring-opening metathesis (co)polymerization (ROMP) of various macromonomers (MMs) using the highly ac
34 heir ring-opening metathesis polymerization (ROMP) and deprotection provide several series of SMAMPs.
35 s in ring-opening metathesis polymerization (ROMP) and ring-closing metathesis (RCM) have been invest
36 n of ring-opening metathesis polymerization (ROMP) and ring-opening polymerization of the amino acid
37 d in ring-opening metathesis polymerization (ROMP) and ring-opening/cross-metathesis (ROCM) processes
38 sion ring-opening metathesis polymerization (ROMP) and used as polymeric supports for organic synthes
39 nium ring-opening metathesis polymerization (ROMP) catalyst under synthetically relevant conditions (
40 sing ring-opening metathesis polymerization (ROMP) for use as efficient alkylating reagents is report
41  the ring-opening metathesis polymerization (ROMP) in aqueous solution were evaluated toward hydrolys
42  and ring opening metathesis polymerization (ROMP) in good to excellent conversion.
43  the ring-opening metathesis polymerization (ROMP) intramolecular backbiting process with the commerc
44  The ring-opening metathesis polymerization (ROMP) is an especially valuable reaction for block copol
45 from ring-opening metathesis polymerization (ROMP) is reported as an effective coupling reagent, scav
46 ieve ring-opening metathesis polymerization (ROMP) mediated by oxidation of organic initiators in the
47  The ring-opening metathesis polymerization (ROMP) of 1,3,5,7-cyclooctatetraene (COT) in the presence
48      Ring-opening metathesis polymerization (ROMP) of dicarbomethoxynorbornadiene (DCMNBD) with 2% 2a
49 s by ring-opening metathesis polymerization (ROMP) of macromonomers (MMs) is highly dependent on the
50 ving ring-opening metathesis polymerization (ROMP) of N-hexyl-exo-norbornene-5,6-dicarboximide initia
51  The ring-opening metathesis polymerization (ROMP) reaction is extraordinarily useful for the prepara
52      Ring opening metathesis polymerization (ROMP) reactions of cyclooctene (COE), bulk-ROMP reaction
53  via ring-opening metathesis polymerization (ROMP) through the employment of a Hamilton receptor-func
54  the ring-opening metathesis polymerization (ROMP) to generate block copolymers that are covalently a
55 ng-opening olefin metathesis polymerization (ROMP) to provide a polypseudorotaxane.
56      Ring-opening metathesis polymerization (ROMP) using Ru==CHPh(Cl)(2)(PCy(3))(DHIMes) (1) as an in
57 free ring-opening metathesis polymerization (ROMP) utilizes organic photoredox mediators as alternati
58  for ring-opening metathesis polymerization (ROMP) with [(H(2)IMes)(3-Br-pyridine)(2)(Cl)(2)Ru=CHPh].
59 e by ring-opening metathesis polymerization (ROMP) with controllable selectivity, ranging from approx
60 d by ring-opening metathesis polymerization (ROMP) with cyclometalated Ru-carbene metathesis catalyst
61 ough ring-opening metathesis polymerization (ROMP) with Mo(NR)(CHCMe2Ph)[OCMe(CF3)2]2 initiators (R =
62  via ring-opening metathesis polymerization (ROMP) with the initiator, (IMesH2)(C5H5N)2(Cl)2RuCHPh.1
63  via ring-opening metathesis polymerization (ROMP), and nitroxide radicals were incorporated at three
64 ore, ring-opening metathesis polymerization (ROMP)-derived monoliths show equivalent preconcentration
65 ving ring-opening metathesis polymerization (ROMP).
66 ) or ring-opening metathesis polymerization (ROMP).
67 ough ring-opening metathesis polymerization (ROMP).
68 e by ring opening metathesis polymerization (ROMP).
69 d by ring-opening metathesis polymerization (ROMP).
70  the ring-opening metathesis polymerization (ROMP).
71 d by ring opening metathesis polymerization (ROMP).
72  via ring-opening metathesis polymerization (ROMP).
73 yzed ring-opening metathesis polymerization (ROMP).
74  polymerization techniques (e.g. ATRP, RAFT, ROMP) that are leading to the creation of sophisticated
75 d bromination reactions to produce saturated ROMP resins with different chemical and physical propert
76 than one type of multivalent ligand and that ROMP is a useful method to synthesize such well-defined
77             To this end, we demonstrate that ROMP can be used to synthesize a block copolymer scaffol
78 ch additionally acts as an inhibitor for the ROMP reaction.
79 ively, the insights provided herein into the ROMP mechanism, monomer design, and homo- and copolymeri
80                       The performance of the ROMP-derived monolithic precolumns was constant over at
81 ap a living polymer chain and regenerate the ROMP initiator with high fidelity.
82 methodology was subsequently extended to the ROMP of 5-bromocyclooct-1-ene and 1,5-cyclooctadiene to
83  The addition of trifluoroacetic acid to the ROMP reaction substantially increased the propagation ra
84  regio- and stereochemical outcomes of these ROMP and ROM reactions were analyzed at the B3LYP/6-31G*
85                           Unlike traditional ROMP with chain transfer, the CTA reacts only with the l
86            The resulting unsaturated ROMP (U-ROMP) resins containing olefin repeat units were chemica
87                                        The U-ROMP resin was also shown to be effective in the solid-p
88                    The resulting unsaturated ROMP (U-ROMP) resins containing olefin repeat units were
89 nene imide) were synthesized either also via ROMP by terminating the polymerization of norbornene oct
90 is and >99% syndiotactic poly(DCMNBD), while ROMP of cyclooctene and 1,5-cyclooctadiene (300 equiv) w

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。