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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
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
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
15 3 was successfully demonstrated in a couple-ROMP-filter protocol utilizing in situ polymerization, a
21 ere isolated, characterized, and employed in ROMP and RCM experiments where they exhibited very low c
23 development of a rate law describing living ROMP initiated by a Grubbs third-generation catalyst tha
27 polymerizable norbornene-on the kinetics of ROMP of polystyrene and poly(lactic acid) MMs initiated
30 is-4-octene as a CTA, the capabilities of PA-ROMP were investigated with a Symyx robotic system, whic
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
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
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
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
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
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
79 ively, the insights provided herein into the ROMP mechanism, monomer design, and homo- and copolymeri
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*
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
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