284
M. Hong
CLA
Classical Lewis adduct
ε-CL
ε-Caprolactone (Scheme 8.1)
DCM
Dichloromethane
DHDM
Double high and double multiple
DMAA
N,N-Dimethyl acrylamide (Scheme 8.1)
Ð
Molecular weight distribution/dispersity
EO
Ethylene oxide (Schemes 8.15)
EMA
Ethyl methacrylate
FLP
Frustrated Lewis pairs
3-F-Py
3-Fluoropyridine (Scheme 8.14)
IN
Indenone (Scheme 8.11)
LPP
Lewis pair polymerization
l-LA
l-Lactide (Scheme 8.1)
MC
Methyl crotonate (Scheme 8.10)
ILP
Interacting Lewis pairs
LB
Lewis base
LA
Lewis acid
MBL
α-Methylene-γ -butyrolactone (Scheme 8.1)
MS
(E,E)-Methyl sorbate (Scheme 8.1)
NHC
N-Heterocyclic carbene
NHO
N-Heterocyclic olefin
OCA
O-Carboxyanhydrides (Scheme 8.13, 8.14)
PO
Propylene oxide (Scheme 8.15)
PDL
ω-Pentadecalactone (Scheme 8.1)
PT
Pentaerythritol (Scheme 8.16)
RO(C)P
Ring-opening (co)polymerization
RT
Room temperature
SFMA
Semifluorinated methacrylate
T g
Glass transition temperature
T d
Onset degradation temperature
T m
Melting temperature
THF
Tetrahydrofuran
TBD
1,5,7-Triazabicyclododecene (Scheme 8.16)
TBGE
tert-Butyl glycidyl ether (Scheme 8.15)
VBMA
4-Vinylbenzyl methacrylate (Scheme 8.1)
VMA
Vinyl methacrylate (Scheme 8.1)
δ-VL
δ-Valerolactone (Scheme 8.1)
MMA
Methyl methacrylate (Scheme 8.1)
DBU
1,8-Diazabicyclo[5.4.0]undec-7-ene (Scheme 8.16)
I
t Bu
1,3-Di-tert-butylimidazolin-2-ylidene (Scheme 8.6)
I
*
Initiation efficiency = M n (calcd)/M n (exptl), where M n (calcd) =
MW(monomer) × [monomer] 0 /[initiator(catalyst)] 0 × conversion
(%) + MW(end groups)
γ MMBL
γ -Methyl-α-methylene-γ -butyrolactone (Scheme 8.1)
MTBD
7-Methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (Scheme 8.16)